Items for Author "Wang, Wayseen"
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Showing 161 items.
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| [亞洲學術期刊] 國科會大專學生研究計畫 |
2020-01-20 |
Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum |
Ch, Chih-Ping; Chen, Chih-Ping; Hs, Chin-Yuan; Hsu, Chin-Yuan; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; Wang, Wayseen; Wang, Wayseen |
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| [亞洲學術期刊] 國科會大專學生研究計畫 |
2020-01-20 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis |
Ch, Chih-Ping; Chen, Chih-Ping; Chen, Chen-Yu; Chen, Chen-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Chen, Li-Feng; Chen, Li-Feng; Wang, Wayseen; Wang, Wayseen |
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| [亞洲學術期刊] 國科會大專學生研究計畫 |
2020-01-20 |
Prenatal diagnosis of concomitant distal 5q duplication and terminal 10q deletion in a fetus with intrauterine growth restriction, congenital diaphragmatic hernia and congenital heart defects |
Ch, Chih-Ping; Chen, Chih-Ping; Hua, Jian-Pei; Huang, Jian-Pei; Che, Shin-Wen; Chen, Shin-Wen; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Wu, Fang-Tzu; Wu, Fang-Tzu; Chen, Wen-Lin; Chen, Wen-Lin; Chen, Li-Feng; Chen, Li-Feng; Wang, Wayseen; Wang, Wayseen |
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| [亞洲學術期刊] 國科會大專學生研究計畫 |
2020-01-20 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo distal 5p deletion and distal 22q duplication |
Ch, Chih-Ping; Chen, Chih-Ping; Hua, Jian-Pei; Huang, Jian-Pei; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; Wu, Fang-Tzu; Wu, Fang-Tzu; Chen, Wen-Lin; Chen, Wen-Lin; Le, Meng-Shan; Lee, Meng-Shan; Wang, Wayseen; Wang, Wayseen |
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| [亞洲學術期刊] 國科會大專學生研究計畫 |
2020-01-20 |
Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic double trisomy involving trisomy 7 and trisomy 20 (48,XY,+7,+20) at amniocentesis |
Ch, Chih-Ping; Chen, Chih-Ping; Lin, Yi-Hui; Lin, Yi-Hui; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; Wu, Fang-Tzu; Wu, Fang-Tzu; Le, Meng-Shan; Lee, Meng-Shan; Chen, Yun-Yi; Chen, Yun-Yi; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2018-10 |
First-trimester cystic hygroma and omphalocele in a fetus with Turner syndrome |
陳持平; Chen, Chih-Ping; Cha, Shu-Yuan; Chang, Shu-Yuan; La, Hui-Shuan; Lau, Hui-Shuan; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Le, Meng-Shan; Lee, Meng-Shan; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2018-10 |
Array comparative genomic hybridization characterization of a 3.3-Mb 17p13.3-p13.2 deletion encompassing YWHAE, CRK, HIC1 and PAFAH1B1 in an 8-year-old girl with Miller-Dieker lissencephaly syndrome, congenital heart defects, growth restriction and developmental delay |
陳持平; Chen, Chih-Ping; Cha, Shu-Yuan; Chang, Shu-Yuan; Li, Shuan-Pei; Lin, Shuan-Pei; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2018-10 |
Detection of hypomethylation of H19 in a pregnancy with limb-body wall complex |
陳持平; Chen, Chih-Ping; Cha, Shu-Yuan; Chang, Shu-Yuan; Hu, Ming-Chao; Huang, Ming-Chao; Ch, Schu-Rern; Chern, Schu-Rern; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2018-08 |
Prenatal diagnosis of a 3.2-Mb 2p16.1-p15 duplication associated with familial intellectual disability |
陳持平; Chen, Chih-Ping; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Chen, Wen-Lin; Chen, Wen-Lin; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2018-08 |
A 13-year-old girl with 18p deletion syndrome presenting Turner syndrome-like clinical features of short stature, short webbed neck, low posterior hair line, puffy eyelids and increased carrying angle of the elbows |
陳持平; Chen, Chih-Ping; Li, Shuan-Pei; Lin, Shuan-Pei; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2018-08 |
A 17-year-old boy with Klinefelter syndrome presenting Marfan syndrome-like clinical features of tall stature, scoliosis, arachnodactyly and subluxation of bilateral elbow joints |
陳持平; Chen, Chih-Ping; Li, Shuan-Pei; Lin, Shuan-Pei; Ch, Schu-Rern; Chern, Schu-Rern; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Chen, Li-Feng; Chen, Li-Feng; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2018-02 |
Prenatal diagnosis of hydrancephaly and enlarged cerebellum and cisterna magna in a fetus with thanatophoric dysplasia type II and a review of prenatal diagnosis of brain anomalies associated with thanatophoric dysplasia |
陳持平; Chen, Chih-Ping; *; Cha, Tung-Yao; Chang, Tung-Yao; Lin, Tan-Wei; Lin, Tan-Wei; Ch, Schu-Rern; Chern, Schu-Rern; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2018-02 |
Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly ;SRTD3; associated with compound heterozygous mutations in DYNC2H1 in a fetus |
陳持平; Chen, Chih-Ping; *; Tsang-Ming, K; Ko, Tsang-Ming; Cha, Tung-Yao; Chang, Tung-Yao; Ch, Schu-Rern; Chern, Schu-Rern; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2018-02 |
Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities |
陳持平; Chen, Chih-Ping; *; Tsang-Ming, K; Ko, Tsang-Ming; Wa, Liang-Kai; Wang, Liang-Kai; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Ya, Chien-Wen; Yang, Chien-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2018-02 |
Late-onset fetal bilateral pleural effusions associated with Down syndrome |
La, Shih-Ting; 陳持平; Chen, Chih-Ping; *; Lin, Chen-Ju; Lin, Chen-Ju; Hs, Chin-Yuan; Hsu, Chin-Yuan; Wu, Peih-Shan; Wu, Peih-Shan; Lee, Chen-Chi; Lee, Chen-Chi; Pan, Chen-Wen; Pan, Chen-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2017-12 |
Prenatal diagnosis of a 1.6-Mb 4p16.3 interstitial microdeletion encompassing FGFRL1 and TACC3 associated with bilateral cleft lip and palate of Wolf-Hirschhorn syndrome facial dysmorphism and short long bones |
陳持平; Chen, Chih-Ping; Chen, Chen-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Ya, Chien-Wen; Yang, Chien-Wen; Chen, Li-Feng; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2017-12 |
Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome |
陳持平; Chen, Chih-Ping; Tsang-Ming, K; Ko, Tsang-Ming; Chen, Yi-Yung; Ch, Schu-Rern; Chern, Schu-Rern; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Ya, Chien-Wen; Yang, Chien-Wen; Pan, Chen-Wen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2017-12 |
Prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis associated with a favorable outcome |
陳持平; Chen, Chih-Ping; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Ya, Chien-Wen; Yang, Chien-Wen; Lee, Chen-Chi; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2017-12 |
Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound |
陳持平; Chen, Chih-Ping; Cha, Tung-Yao; Chang, Tung-Yao; Hung, Fang-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Lee, Chen-Chi; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2017-12 |
Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1 |
陳持平; Chen, Chih-Ping; Hs, Chih-Heng; Hsieh, Chih-Heng; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Ya, Chien-Wen; Yang, Chien-Wen; Lee, Chen-Chi; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2017-12 |
Fetoplacental cytogenetic discrepancy in a pregnancy with fetal mosaic tetrasomy 12p and Pallister-Killian syndrome detected by amniocentesis |
陳持平; Chen, Chih-Ping; Wa, Liang-Kai; Wang, Liang-Kai; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Chen, Li-Feng; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2017-10 |
Application of non-invasive prenatal testing in late gestation in a pregnancy associated with intrauterine growth restriction and trisomy 22 confined placental mosaicism |
陳持平; Chen, Chih-Ping; Tsai, Chris; Tsai, Chris; Li, Ming-Huei; Lin, Ming-Huei; Ch, Schu-Rern; Chern, Schu-Rern; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chen, Wen-Lin; Pan, Chen-Wen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-12 |
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22->q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder and in |
陳持平; Chen, Chih-Ping; *; Li, Shuan-Pei; Lin, Shuan-Pei; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Ya, Chien-Wen; Yang, Chien-Wen; Le, Meng-Shan; Lee, Meng-Shan; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-12 |
Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality |
陳持平; Chen, Chih-Ping; *; Fu, Chung-Hu; Fu, Chung-Hu; Lin, Yi-Hui; Lin, Yi-Hui; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-12 |
Detection of a novel c.7106_7110delinsT heterozygous mutation in the FLNA gene in an asymptomatic mother with periventricular nodular heterotopia during prenatal genetic counseling |
陳持平; Chen, Chih-Ping; *; Ch, Schu-Rern; Chern, Schu-Rern; Ch, Nan-Chang; Chiu, Nan-Chang; Liu, Yu-Peng; Liu, Yu-Peng; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-12 |
Prenatal diagnosis of low-level mosaicism for trisomy 12 associated with a favorable pregnancy outcome |
陳持平; Chen, Chih-Ping; *; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-12 |
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12->q13.1::) associated with phenotypic abnormalities |
陳持平; Chen, Chih-Ping; *; Li, Shuan-Pei; Lin, Shuan-Pei; Lin, Yi-Hui; Lin, Yi-Hui; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Ya, Chien-Wen; Yang, Chien-Wen; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-10 |
Molecular cytogenetic characterization of Xp22.32->pter deletion and Xq26.3->qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq)inv(X)(p22.3q26.3), a hypoplastic left heart, short stature and maternal X chromosome pericentric inversion |
陳持平; Chen, Chih-Ping; *; Chen, Chen-Yu; Chen, Chen-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Town, Dai-Dyi; Town, Dai-Dyi; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-10 |
Mosaic trisomy 17 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review |
陳持平; Chen, Chih-Ping; *; Wa, Liang-Kai; Wang, Liang-Kai; Ch, Schu-Rern; Chern, Schu-Rern; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Wu, Peih-Shan; Wu, Peih-Shan; Town, Dai-Dyi; Town, Dai-Dyi; Pan, Chen-Wen; Pan, Chen-Wen; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-10 |
Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome |
陳持平; Chen, Chih-Ping; *; Li, Shuan-Pei; Lin, Shuan-Pei; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Town, Dai-Dyi; Town, Dai-Dyi; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-10 |
Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentirc inversion |
陳持平; Chen, Chih-Ping; *; Tsang-Ming, K; Ko, Tsang-Ming; Su, Yi-Ning; Su, Yi-Ning; Wa, Liang-Kai; Wang, Liang-Kai; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Che, Shin-Wen; Town, Dai-Dyi; Town, Dai-Dyi; Chen, Li-Feng; Chen, Li-Feng; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-10 |
Prenatal imaging findings of a rapidly involuting congenital hemangioma (RICH) over right flank in a fetus with a favorable outcome |
陳持平; Chen, Chih-Ping; *; Chen, Chen-Yu; Chen, Chen-Yu; Cha, Tung-Yao; Chang, Tung-Yao; Yang, Hsiu-Yu; Yang, Hsiu-Yu; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-08 |
Prenatal diagnosis of partial monosomy 5p (5p15.1->pter) and partial trisomy 7p (7p15.2->pter) associated with cystic hygroma, abnormal skull development and ventriculomegaly |
陳持平; Chen, Chih-Ping; *; Wa, Liang-Kai; Wang, Liang-Kai; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Ko, Kevin; Ko, Kevin; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Le, Meng-Shan; Lee, Meng-Shan; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-08 |
Prenatal diagnosis and molecular cytogenetic characterization of a de novo unbalanced reciprocal translocation of der(9)t(9;14)(p24.2;q32.11) associated with 9p terminal deletion and 14q distal duplication |
陳持平; Chen, Chih-Ping; *; Lin, Chen-Ju; Lin, Chen-Ju; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Chen, Li-Feng; Chen, Li-Feng; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-08 |
Rapid diagnosis of pseudomosaicism in a case of level II mosaicism for trisomy 5 in a single colony from an in situ culture of amniocytes and a review of mosaic trisomy 5 at amniocentesis |
陳持平; Chen, Chih-Ping; *; Ch, Shing-Jyh; Chang, Shing-Jyh; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Ya, Chien-Wen; Yang, Chien-Wen; Pan, Chen-Wen; Pan, Chen-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-06 |
Molecular cytogenetic characterization of inv dup del;8p; in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction |
陳持平; Chen, Chih-Ping; *; Tsang-Ming, K; Ko, Tsang-Ming; Huan, Wen-Chu; Huang, Wen-Chu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Chen-Wen Pan; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-06 |
Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay and speech delay |
陳持平; Chen, Chih-Ping; *; Chiang, Sheng; Chiang, Sheng; Kung-Liahng; Wang, Kung-Liahng; Cho, Fu-Nan; Cho, Fu-Nan; Chen, Ming; Chen, Ming; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Shin-Wen Chen; Shun-Ping Chang; Chen, Weu-Lin; Chen, Weu-Lin; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-06 |
22q13 deletion syndrome in a fetus associated with microtia, hemivertebrae and congenital heart defects on prenatal ultrasound |
陳持平; Chen, Chih-Ping; *; Cha, Tung-Yao; Chang, Tung-Yao; Wa, Liang-Kai; Wang, Liang-Kai; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Chen, Weu-Lin; Chen, Weu-Lin; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-06 |
Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction |
陳持平; Chen, Chih-Ping; *; Tsang-Ming, K; Ko, Tsang-Ming; Huan, Wen-Chu; Huang, Wen-Chu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Chen-Wen Pan; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-04 |
Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetrology of Fallot |
陳持平; Chen, Chih-Ping; *; Chen, Chen-Yu; Chen, Chen-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Chen, Li-Feng; Chen, Li-Feng; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-04 |
Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes |
陳持平; Chen, Chih-Ping; *; Wan, Yeou-Lih; Wang, Yeou-Lih; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Chen, Li-Feng; Chen, Li-Feng; Le, Meng-Shan; Lee, Meng-Shan; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-04 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p ;3p26.3->pter; and partial trisomy 16q ;16q23.1->qter; |
陳持平; Chen, Chih-Ping; *; Hung, Fang-Yu; Hung, Fang-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-04 |
Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome |
陳持平; Chen, Chih-Ping; *; Tsang-Ming, K; Ko, Tsang-Ming; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Chen, Li-Feng; Chen, Li-Feng; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-04 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3->pter) and partial trisomy 16q (16q23.1->qter) |
陳持平; Chen, Chih-Ping; *; Hung, Fang-Yu; Hung, Fang-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2016-02 |
Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion |
Chen, Yen-Ni; Chen, Yen-Ni; 陳持平*; Tsang-Ming, K; Ko, Tsang-Ming; Wa, Liang-Kai; Wang, Liang-Kai; Wu, Pei-Chen; Wu, Pei-Chen; Cha, Tung-Yao; Chang, Tung-Yao; Wu, Peih-Shan; Wu, Peih-Shan; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
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Detection of no isochromosome 20q by interphase fluorescence in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis |
Su, 陳持平*、Jun-Wei; Su, Jun-Wei; Ch, Schu-Rern; Chern, Schu-Rern; Kuo, Yu-Ling; Kuo, Yu-Ling; Wu, Peih-Shan; Wu, Peih-Shan; Le, Meng-Shan; Lee, Meng-Shan; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
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Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diap |
Wan, 陳持平*、Yeou-Lih; Wang, Yeou-Lih; Ch, Schu-Rern; Chern, Schu-Rern; Liu, Yu-Peng; Liu, Yu-Peng; Pe, Cheng-Ran; Peng, Cheng-Ran; Kuo, Yu-Ling; Kuo, Yu-Ling; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
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Detection of de novo secondary trisomy 13 due to isochromosome ;13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma |
陳持平*、Tsang-Ming, K; Ko, Tsang-Ming; Hu, Ming-Chao; Huang, Ming-Chao; Ch, Schu-Rern; Chern, Schu-Rern; Lin, Tan-Wei; Lin, Tan-Wei; Cha, Tung-Yao; Chang, Tung-Yao; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2015-04 |
First-trimester diagnosis of recurrent omphalocele associated with fetal trisomy 18 but without parental mosaicism |
陳持平*; Wa, Liang-Kai; Wang, Liang-Kai; Ch, Schu-Rern; Chern, Schu-Rern; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Yen-Ni; Chen, Yen-Ni; Pan, Chen-Wen; Pan, Chen-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2015-02 |
Detection of no isochromosome 20q by interphase fluorescence in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis |
陳持平*; Su, Jun-Wei; Su, Jun-Wei; Ch, Schu-Rern; Chern, Schu-Rern; Kuo, Yu-Ling; Kuo, Yu-Ling; Wu, Peih-Shan; Wu, Peih-Shan; Le, Meng-Shan; Lee, Meng-Shan; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2015-02 |
Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diap |
陳持平*; Wan, Yeou-Lih; Wang, Yeou-Lih; Ch, Schu-Rern; Chern, Schu-Rern; Liu, Yu-Peng; Liu, Yu-Peng; Pe, Cheng-Ran; Peng, Cheng-Ran; Kuo, Yu-Ling; Kuo, Yu-Ling; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2015-02 |
Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma |
陳持平*; Tsang-Ming, K; Ko, Tsang-Ming; Hu, Ming-Chao; Huang, Ming-Chao; Ch, Schu-Rern; Chern, Schu-Rern; Lin, Tan-Wei; Lin, Tan-Wei; Cha, Tung-Yao; Chang, Tung-Yao; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2015-02 |
Detection of de novo secondary trisomy 13 due to isochromosome ;13q;13q; of paternal origin in a pregnancy with fetal cystic hygroma |
陳持平; Tsang-Ming, K; Ko, Tsang-Ming; Hu, Ming-Chao; Huang, Ming-Chao; Ch, Schu-Rern; Chern, Schu-Rern; Lin, Tan-Wei; Lin, Tan-Wei; Cha, Tung-Yao; Chang, Tung-Yao; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2015-02 |
Detection of no isochromosome 20q by interphase fluorescent in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis |
陳持平*; Su, Jun-Wei; Su, Jun-Wei; Ch, Schu-Rern; Chern, Schu-Rern; Kuo, Yu-Ling; Kuo, Yu-Ling; Wu, Peih-Shan; Wu, Peih-Shan; Le, Meng-Shan; Lee, Meng-Shan; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2015-02 |
Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q ; of paternal origin in a pregnancy with fetal cystic hygroma |
; Ko, Tsang-Ming; Hu, Ming-Chao; Huang, Ming-Chao; Ch, Schu-Rern; Chern, Schu-Rern; Lin, Tan-Wei; Lin, Tan-Wei; Cha, Tung-Yao; Chang, Tung-Yao; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2014-03 |
Detection of altered methylation status at 11p15 and 7q32 in placental mesenchymal dysplasia |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Su, Yi-Ning; Li, Ming-Huei; Lin, Ming-Huei; Wa, Tao-Yeuan; Wang, Tao-Yeuan; Ch, Schu-Rern; Chern, Schu-Rern; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Yu-Ting; Chen, Yu-Ting; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2014-03 |
A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2 duplication detected by array comparative genomic hybridization in an adolescent girl with autism and difficulty in self-care of menstruation |
陳持平; Chen, Chih-Ping; Li, Shuan-Pei; Lin, Shuan-Pei; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2014-03 |
Mosaic tetrasomy 9p at amniocentesis: prenatal diagnosis, molecular cytogenetic characterization and literature review |
陳持平; Chen, Chih-Ping; Wa, Liang-Kai; Wang, Liang-Kai; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yu-Ting; Chen, Yu-Ting; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Wen-Lin; Chen, Wen-Lin; Le, Meng-Shan; Lee, Meng-Shan; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2014-03 |
Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived by ICSI and IVF-ET |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Su, Yi-Ning; Che, Shee-Uan; Chen, Shee-Uan; Cha, Tung-Yao; Chang, Tung-Yao; Wu, Pei-Chen; Wu, Pei-Chen; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Kuo, Yu-Ling; Kuo, Yu-Ling; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2014-03 |
Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid diagnosis of true mosaicism in a case of level II mosaicism involving trisomy 21 in a single colony from an in situ culture of amniocytes |
陳持平; Chen, Chih-Ping; Wang, Pu-Tsui; Wang, Pu-Tsui; Li, Shuan-Pei; Lin, Shuan-Pei; Ch, Schu-Rern; Chern, Schu-Rern; Chen, Yu-Ting; Chen, Yu-Ting; Wu, Peih-Shan; Wu, Peih-Shan; Kuo, Yu-Ling; Kuo, Yu-Ling; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2014-03 |
Directly transmitted 4.5-Mb triplication of 4q12-q13.1: prenatal diagnosis and molecular cytogenetic characterization |
陳持平; Chen, Chih-Ping; Li, Ming-Huei; Lin, Ming-Huei; Ch, Schu-Rern; Chern, Schu-Rern; Chen, Yu-Ting; Chen, Yu-Ting; Wu, Peih-Shan; Wu, Peih-Shan; Kuo, Yu-Ling; Kuo, Yu-Ling; Le, Meng-Shan; Lee, Meng-Shan; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2014-03 |
Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid confirmation of low-level mosaicism for tetrasomy 18p |
陳持平; Chen, Chih-Ping; Lin, Chen-Ju; Lin, Chen-Ju; Tsang-Ming, K; Ko, Tsang-Ming; Ch, Schu-Rern; Chern, Schu-Rern; Chen, Yu-Ting; Chen, Yu-Ting; Wu, Peih-Shan; Wu, Peih-Shan; Kuo, Yu-Ling; Kuo, Yu-Ling; Le, Meng-Shan; Lee, Meng-Shan; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2014-03 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15 |
陳持平; Chen, Chih-Ping; Chen, Ming; Chen, Ming; Su, Yi-Ning; Chern, Schu-Rern; Wu, Peih-Shan; Ch, Shun-Ping; Kuo, Yu-Ling; Chen, Wen-Lin; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2014-02 |
Array CGH characterization of an unbalanced X-autosome translocation associated with Xq27.2-qter deletion, 11q24.3-qter duplication and Xq22.3-q27.1 duplication in a girl with primary amenorrhea and mental retardation |
陳持平; Chen, Chih-Ping; Li, Shuan-Pei; Lin, Shuan-Pei; Ch, Schu-Rern; Chern, Schu-Rern; Kuo, Yu-Ling; Kuo, Yu-Ling; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yu-Ting; Chen, Yu-Ting; Le, Meng-Shan; Lee, Meng-Shan; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
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Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review |
陳持平; Chen, Chih-Ping; Chen, Ming; Chen, Ming; Su, Yi-Ning; Su, Yi-Ning; Hua, Jian-Pei; Huang, Jian-Pei; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Ch, Shun-Ping; Chang, Shun-Ping; Chen, Li-Feng; Chen, Li-Feng; Pan, Chen-Wen; Pan, Chen-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
|
An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy |
陳持平; Chen, Chih-Ping; Li, Shuan-Pei; Lin, Shuan-Pei; Liu, Yu-Peng; Liu, Yu-Peng; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Chen, Yu-Ting; Chen, Yu-Ting; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
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Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review |
陳持平; Chen, Chih-Ping; Hua, Jian-Pei; Huang, Jian-Pei; Chen, Yi-Yung; Chen, Yi-Yung; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Chen, Yu-Ting; Chen, Yu-Ting; Chen, Wen-Lin; Chen, Wen-Lin; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
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Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes |
陳持平; Chen, Chih-Ping; Hua, Jian-Pei; Huang, Jian-Pei; Chen, Yi-Yung; Chen, Yi-Yung; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Pan, Chen-Wen; Pan, Chen-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
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Prenatal diagnosis of mosaic trisomy 2 associated with abnormal maternal serum screening, oligohydramnios, intrauterine growth restriction, ventricular septal defect, preaxial polydactyly and facial dysmorphism |
陳持平; Chen, Chih-Ping; Chen, Yi-Yung; Chen, Yi-Yung; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Chen, Yu-Ting; Chen, Yu-Ting; Lee, Chen-Chi; Lee, Chen-Chi; Chen, Li-Feng; Li-Feng Chen,; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
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De novo unbalanced translocation resulting in monosomy for distal 5p (5p14.1->pter) and 14q (14q32.31->qter) associated with fetal nuchal edema, microcephaly, intrauterine growth restriction and single umbilical artery: prenatal diagnosis and molecular |
陳持平; Chen, Chih-Ping; Fu, Chung-Hu; Fu, Chung-Hu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Lee, Chen-Chi; Lee, Chen-Chi; Le, Meng-Shan; Lee, Meng-Shan; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
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Detection of maternal transmission of a splicing mutation in the TSC2 gene following prenatal diagnosis of fetal cardiac rhabdomyomas mimicking congenital cystic adenomatoid malformation of the lung and cerebral tubers and awareness of a family history of |
陳持平; Chen, Chih-Ping; Cha, Tung-Yao; Chang, Tung-Yao; Guo, Wan-Yuo; Guo, Wan-Yuo; Su, Yi-Ning; Su, Yi-Ning; Chen, Yi-Yung; Chen, Yi-Yung; Ch, Schu-Rern; Chern, Schu-Rern; Su, Jun-Wei; Su, Jun-Wei; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
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Rapid detection of K650E mutation in FGFR3 using uncultured amniocytes in a pregnancy affected with fetal cloverleaf skull, occipital pseudoencephalocele, ventriculomegaly, straight short femurs and thanatophoric dysplasia type II |
陳持平; Chen, Chih-Ping; Cha, Tung-Yao; Chang, Tung-Yao; Li, Ming-Huei; Lin, Ming-Huei; Ch, Schu-Rern; Chern, Schu-Rern; Su, Jun-Wei; Su, Jun-Wei; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
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Mosaic trisomy 14 at amniocentesis: prenatal diagnosis and literature review |
陳持平; Chen, Chih-Ping; Wang, Kuo-Gon; Wang, Kuo-Gon; Tsang-Ming, K; Ko, Tsang-Ming; Ch, Schu-Rern; Chern, Schu-Rern; Su, Jun-Wei; Su, Jun-Wei; Town, Dai-Dyi; Town, Dai-Dyi; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
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Application of interphase fluorescence in situ hybridization to uncultured amniocytes for differential diagnosis of pseudomosaicism from true mosaicism in mosaic isochromosome 20q detected at amniocentesis |
陳持平; Chen, Chih-Ping; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Chen, Yu-Ting; Chen, Yu-Ting; Chen, Li-Feng; Chen, Li-Feng; Pan, Chen-Wen; Pan, Chen-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
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Prenatal diagnosis of mosaic trisomy 12 associated with congenital overgrowth |
陳持平; Chen, Chih-Ping; Ch, Shing-Jyh; Chang, Shing-Jyh; Su, Jun-Wei; Su, Jun-Wei; Chen, Yu-Ting; Chen, Yu-Ting; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2013-10 |
An interstitial deletion of 8q23.3-q24.22 associated with Langer-Giedion syndrome, Cornelia de Lange syndrome and epilepsy |
陳持平; Chen, Chih-Ping; Li, Shuan-Pei; Lin, Shuan-Pei; Liu, Yu-Peng; Liu, Yu-Peng; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Chen, Yu-Ting; Chen, Yu-Ting; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2013-10 |
Mosaic small supernumerary marker chromosome 1 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review |
陳持平; Chen, Chih-Ping; Chen, Ming; Chen, Ming; Su, Yi-Ning; Su, Yi-Ning; Hua, Jian-Pei; Huang, Jian-Pei; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Ch, Shun-Ping; Chang, Shun-Ping; Chen, Li-Feng; Chen, Li-Feng; Pan, Chen-Wen; Pan, Chen-Wen; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2013-09 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome |
陳持平; Chen, Chih-Ping; Tsang-Ming, K; Ko, Tsang-Ming; Chen, Yi-Yung; Su, Jun-Wei; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2013-07 |
6p21.2-p12.3 deletion detected by aCGH in an 8-year-old girl with cleidocranial dysplasia, psychomotor developmental delay and poor wound healing |
陳持平; Chen, Chih-Ping; Li, Shuan-Pei; Lin, Shuan-Pei; Liu, Yu-Peng; Liu, Yu-Peng; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yu-Ting; Chen, Yu-Ting; Su, Jun-Wei; Su, Jun-Wei; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2013-07 |
Cri-du-chat (5p-) syndrome presenting with cerebellar hypoplasia and hypospadias: prenatal diagnosis and aCGH characterization using uncultured amniocytes |
陳持平; Chen, Chih-Ping; Hu, Ming-Chao; Huang, Ming-Chao; Chen, Yi-Yung; Chen, Yi-Yung; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yu-Ting; Chen, Yu-Ting; Su, Jun-Wei; Su, Jun-Wei; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2013-06 |
Ring chromosome 21 presenting with sacrococcygeal teratoma: prenatal diagnosis, molecular cytogenetic characterization and literature review |
陳持平; Chen, Chih-Ping; Cheng, Po-Jen; Cheng, Po-Jen; Shuenn-Dyh, C; Chang, Shuenn-Dyh; Lee, Yi-Xuan; Lee, Yi-Xuan; Sh, Jin-Chung; Shih, Jin-Chung; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Chen, Li-Feng; Chen, Li-Feng; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2013-06 |
A boy with cleft palate, hearing impairment, microcephaly, micrognathia and psychomotor retardation and a microdeletion in 6p25.3 involving the DUSP22 gene |
陳持平; Chen, Chih-Ping; Li, Shuan-Pei; Lin, Shuan-Pei; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Wang, Wayseen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2013-04 |
Prenatal diagnosis of ring chromosome 2 with lissencephaly and 2p25.3 and 2q37.3 microdeletions detected using array comparative genomic hybridization |
陳持平; Chen, Chih-Ping; Lin, Chen-Ju; Lin, Chen-Ju; Cha, Tung-Yao; Chang, Tung-Yao; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yu-Ting; Chen, Yu-Ting; Su, Jun-Wei; Su, Jun-Wei; Lee, Chen-Chi; Lee, Chen-Chi; Chen, Li-Feng; Chen, Li-Feng; Wang, Wayseen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2013-03 |
Prenatal diagnosis of partial trisomy 3q (3q27.3->qter) and partial monosomy 14q (14q31.3->qter) of paternal origin associated with fetal hypotonia, arthrogryposis, scoliosis and hyperextensible joints |
陳持平; Chen, Chih-Ping; Cha, Yao-Lung; Chang, Yao-Lung; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Su, Jun-Wei; Su, Jun-Wei; Chen, Wen-Lin; Chen, Wen-Lin; Chen, Li-Feng; Chen, Li-Feng; Wang, Wayseen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2013-03 |
Discrepancy in the trisomy mosaicism level between cultured amniocytes and uncultured amniocytes in prenatally detected mosaic trisomy 20 |
陳持平; Chen, Chih-Ping; Shuenn-Dyh, C; Chang, Shuenn-Dyh; Chueh, Ho-Yen; Chueh, Ho-Yen; Su, Yi-Ning; Su, Yi-Ning; Ch, Schu-Rern; Chern, Schu-Rern; Su, Jun-Wei; Su, Jun-Wei; Chen, Yu-Ting; Chen, Yu-Ting; Chen, Li-Feng; Chen, Li-Feng; Le, Meng-Shan; Lee, Meng-Shan; Wang, Wayseen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2013-03 |
Mosaic trisomy 12 at amniocentesis: prenatal diagnosis and molecular genetic analysis |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Su, Yi-Ning; Su, Jun-Wei; Su, Jun-Wei; Ch, Schu-Rern; Chern, Schu-Rern; Chen, Yu-Ting; Chen, Yu-Ting; Chen, Li-Feng; Chen, Li-Feng; Wang, Wayseen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2013-03 |
Placental mesenchymal dysplasia associated with antepartum hemorrhage, subchorionic hematoma and intrauterine growth restriction |
陳持平; Chen, Chih-Ping; Hs, Chin-Yuan; Hsu, Chin-Yuan; Su, Yi-Ning; Su, Yi-Ning; Wa, Tao-Yeuan; Wang, Tao-Yeuan; Chen, Yi-Yung; Chen, Yi-Yung; Ch, Schu-Rern; Chern, Schu-Rern; Su, Jun-Wei; Su, Jun-Wei; Wang, Wayseen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2013-03 |
Prenatal diagnosis of a missense mutation of c.2279G>A, Gly760Glu in exon 37 of COL1A2 in a fetus with familial osteogenesis imperfecta type IV and favorable outcome |
陳持平; Chen, Chih-Ping; Li, Shuan-Pei; Lin, Shuan-Pei; Su, Yi-Ning; Su, Yi-Ning; Ch, Schu-Rern; Chern, Schu-Rern; Su, Jun-Wei; Su, Jun-Wei; Wang, Wayseen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2013-03 |
Prenatal diagnosis of and molecular cytogenetic characterization of a de novo interstitial duplication of 11q (11q22.3->q23.3) associated with abnormal maternal serum biochemistry |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Su, Yi-Ning; Li, Shuan-Pei; Lin, Shuan-Pei; Ch, Schu-Rern; Chern, Schu-Rern; Su, Jun-Wei; Su, Jun-Wei; Chen, Yu-Ting; Chen, Yu-Ting; Le, Meng-Shan; Lee, Meng-Shan; Wang, Wayseen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2013-03 |
Prenatal diagnosis of recurrent autosomal dominant osteogenesis imperfecta associated with unaffected parents and paternal gonadal mosaicism |
陳持平; Chen, Chih-Ping; Li, Shuan-Pei; Lin, Shuan-Pei; Su, Yi-Ning; Su, Yi-Ning; Ch, Schu-Rern; Chern, Schu-Rern; Su, Jun-Wei; Su, Jun-Wei; Wang, Wayseen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2013-01 |
Array comparative genomic hybridization characterization of prenatally detected de novo apparently balanced reciprocal translocations with or without genomic imbalance in other chromosome |
陳持平; Chen, Chih-Ping; Chen, Ming; Chen, Ming; Ma, Gwo-Chin; Ma, Gwo-Chin; Su, Yi-Ning; Su, Yi-Ning; Tsang-Ming, K; Ko, Tsang-Ming; Lin, Yi-Hui; Lin, Yi-Hui; Wang, Wayseen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2012-09 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2 |
陳持平; Chen, Chih-Ping; Jun-Wei Su,; Alan Hwa-Ruey Hsieh,; Hsieh, Alex Hwa-Jiun; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2012-09 |
Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase FISH, QF-PCR and aCGH on uncultured amniocytes in a pregnancy with fetal pyelectasis |
陳持平; Chen, Chih-Ping; Chen-Wen Pan,; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2012-09 |
Rapid positive confirmation of trisomy 21 mosaicism at amniocentesis by interphase FISH, QF-PCR and aCGH on uncultured amniocytes |
陳持平; Chen, Chih-Ping; Dai-Dyi Town,; Wen-Lin Chen,; Chen, Li-Feng; Meng-Shan Lee,; Pan, Chen-Wen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2012-06 |
Inv dup del(10q): Identification by fluorescence in situ hybridization and array comparative genomic hybridization in a fetus with two concurrent chromosomal rearrangements |
陳持平; Chen, Chih-Ping; Jun-Wei Su,; Chen-Chi Lee,; Town, Dai-Dyi; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2012-03 |
Unexplained shortening of the long bones in the third trimester as the only prenatal feature in a male fetus with 45,X/46,X,r(Y) mosaicism |
陳持平; Chen, Chih-Ping; Yu-Ting Chen,; Chen, Li-Feng; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2011-12 |
A de novo duplication of chromosome 21q22.11->qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings |
陳持平; Chen, Chih-Ping; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2011-09 |
Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization and perinatal findings in a fetus with dup(15)(q26.2q26.3) |
陳持平; Chen, Chih-Ping; Li-Feng Chen,; Adam Hwa-Ming Hsieh,; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2011-09 |
Mosaic supernumerary r(1)(p13.2q23.3) in a 10-year-old girl with epilepsy, facial asymmetry, psychomotor retardation, kyphoscoliosis, dermatofibrosarcoma and multiple exostoses |
陳持平; Chen, Chih-Ping; Chen-Chi Lee,; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2011-06 |
Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis |
陳持平; Chen, Chih-Ping; Chen-Chi Lee,; Wen-Lin Chen,; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2011-03 |
Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations |
陳持平; Chen, Chih-Ping; Yi-Yung Chen,; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-12 |
A 5.3-Mb duplication of 9p12->p13.1 characterized by array CGH in a female infant with developmental delay |
陳持平; Chen, Chih-Ping; Lin, Shuan-Pei; Chern, Schu-Rern; Tsai, Fuu-Jen; Lee, Chen-Chi; Pan, Chen-Wen; Wu, Pei-Chen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-12 |
Balanced reciprocal translocations at amniocentesis |
陳持平; Chen, Chih-Ping; Wu, Pei-Chen; Su, Yi-Ning; Chern, Schu-Rern; Tsai, Fuu-Jen; Lee, Chen-Chi; Town, Dai-Dyi; Chen, Wen-Lin; Chen, Li-Feng; Pan, Chen-Wen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-12 |
Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings |
陳持平; Chen, Chih-Ping; Chen, Ming; Su, Yi-Ning; Hsu, Chin-Yuan; Tsai, Fuu-Jen; Chern, Schu-Rern; Wu, Pei-Chen; Lee, Chen-Chi; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-12 |
Microvillus inclusion disease: prenatal ultrasound findings, molecular diagnosis and genetic counseling of congenital diarrhea |
陳持平; Chen, Chih-Ping; Chiang, Ming-Chou; Wang, Tzu-Hao; Hsueh, Chuen; Chang, Shueen-Dyh; Tsai, Fuu-Jen; Wang, Chao-Ning; Chern, Schu-Rern; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-12 |
Partial trisomy 10q (10q25.1->qter) and partial monosomy 13q (13q34->qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Tsai, Fuu-Jen; Hsu, Chin-Yuan; Chern, Schu-Rern; Wu, Pei-Chen; Lee, Chen-Chi; Chen, Wen-Lin; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-12 |
Partial trisomy 16p (16p12.2->pter) and partial monosomy 22q (22q13.31->qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Young, Richard Shih-Hung; Tsai, Fuu-Jen; Wu, Pei-Chen; Chern, Schu-Rern; Town, Dai-Dyi; Pan, Chen-Wen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-12 |
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8 |
陳持平; Chen, Chih-Ping; Chen, Ming; Ko, Tsang-Ming; Ma, Gwo-Chin; Tsai, Fuu-Jen; Tsai, Ming-Song; Wu, Pei-Chen; Lee, Chen-Chi; Che, Li-Feng; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-12 |
Prenatal diagnosis of partial monosomy 1q (1q42.3->qter) associated with hydrocephalus and corpus callosum agenesis |
陳持平; Chen, Chih-Ping; Chern, Schu-Rern; Tsai, Fuu-Jen; Lin, Hung-Hung; Wu, Pei-Chen; Lee, Chen-Chi; Pan, Chen-Wen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-12 |
Recurrent distal 16q duplication and terminal 22q deletion: prenatal diagnosis and genetic counseling |
陳持平; Chen, Chih-Ping; Huang, Ming-Chao; Su, Yi-Ning; Tsai, Fuu-Jen; Wu, Pei-Chen; Lee, Chen-Chi; Town, Dai-Dyi; Pan, Chen-Wen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-09 |
A de novo 7.9 Mb deletion in 22q13.2->qter in a boy with autistic features, epilepsy, developmental delay atopic dermatitis and abnormal immunological findings |
陳持平; Chen, Chih-Ping; Lin, Shuan-Pei; Chern, Schu-Rern; Tsai, Fuu-Jen; Wu, Pei-Chen; Lee, Chen-Chi; Chen, Yu-Ting; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-09 |
Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization |
陳持平; Chen, Chih-Ping; Guo, Yung-Ting; Lin, Shuan-Pei; Su, Yi-Ning; Chen, Yann-Jang; Hseuh, Rui-Yuan; Lin, Yi-Hui; Wu, Pei-Chen; Lee, Chen-Chi; Chen, Yu-Ting; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-09 |
Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Chern, Schu-Rern; Hwu, Yu-Ming; Lin, Shuan-Pei; Hsu, Chyong-Hsin; Tsai, Fuu-Jen; Wang, Tao-Yeuan; Wu, Pei-Chen; Lee, Chen-Chi; Chen, Yu-Ting; Chen, Li-Feng; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-09 |
Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses |
陳持平; Chen, Chih-Ping; Lin, Hsien-Ming; Su, Yi-Ning; Chern, Schu-Rern; Tsai, Fuu-Jen; Wu, Pei-Chen; Lee, Chen-Chi; Chen, Yu-Ting; Lee, Meng-Shan; Pan, Chen-Wen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-09 |
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21 |
陳持平; Chen, Chih-Ping; Lin, Chyi-Chyang; Ko, Tsang-Ming; Tsai, Fuu-Jen; Chern, Schu-Rern; Lee, Chen-Chi; Chen, Yu-Ting; Wu, Pei-Chen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-09 |
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22 |
陳持平; Chen, Chih-Ping; Lin, Chyi-Chyang; Su, Yi-Ning; Tsai, Fuu-Jen; Chern, Schu-Rern; Lee, Chen-Chi; Chen, Wen-Ling; Chen, Li-Feng; Wu, Pei-Chen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-09 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3->pter) and partial monosomy 13q (13q33.3->qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly |
陳持平; Chen, Chih-Ping; Chen, Ming; Su, Yi-Ning; Tsai, Fuu-Jen; Chern, Schu-Rern; Hsu, Chin-Yuan; Wu, Pei-Chen; Town, Dai-Dyi; Lee, Dong-Jay; Ma, Gwo-Chin; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-09 |
Prenatal diagnosis of persistent cloaca with hydrometrocolpos and ascites by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy |
陳持平; Chen, Chih-Ping; Liu, Yu-Peng; Chang, Tung-Yao; Tsai, Fuu-Jen; Chen, Chen-Yu; Wu, Pei-Chen; Chen, Teresa Hsiao-Tien; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-09 |
Prenatal diagnosis of rhabdomyomas and cerebral tuberous sclerosis by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy associated with a frameshift mutation in the TSC2 gene |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Chang, Tung-Yao; Liu, Yu-Peng; Tsai, Fuu-Jen; Chen, Ming-Ren; Hwang, Jonathan Kwei; Chen, Teresa Hsiao-Tien; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-09 |
Prenatal diagnosis of satellited 21q derived from pericentric inversion involving the satellite stalk region and terminal 21q |
陳持平; Chen, Chih-Ping; Tsai, Fuu-Jen; Lee, Chen-Chi; Chen, Wen-Lin; Pan, Chen-Wen; Wu, Pei-Chen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-07 |
Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2->q24.3 in a girl with autistic features and developmental delay |
陳持平; Chen, Chih-Ping; Lin, Shuan-Pei; Chern, Schu-Rern; Chen, Yann-Jang; Tsai, Fuu-Jen; Wu, Pei-Chen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-06 |
Apert syndrome associated with upper airway obstruction and gastroesophageal reflux presenting polyhydramnios in the third trimester |
陳持平; Chen, Chih-Ping; Lin, Shuan-Pei; Su, Yi-Ning; Chen, Chen-Yu; Tsai, Fuu-Jen; Liu, Yu-Peng; Chern, Schu-Rern; Wu, Pei-Chen; Chen, Hsaio-En Cindy; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-06 |
Deletion 2q37.3->qter and duplication 15q24.3->qter characterized by array CGH in a girl with epilepsy and dysmorphic features |
陳持平; Chen, Chih-Ping; Lin, Shuan-Pei; Chern, Schu-Rern; Tsai, Fuu-Jen; Wu, Pei-Chen; Lee, Chen-Chi; Chen, Li-Feng; Lee, Meng-Shan; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-06 |
Detection and comparison of the levels of cytomegalovirus DNA in amniotic fluid and fetal ascites in a second-trimester fetus with massive ascites, hyperechogenic bowel, ventriculomegaly and intrauterine growth restriction |
陳持平; Chen, Chih-Ping; Chern, Schu-Rern; Wang, Tao-Yeuan; Tsai, Fuu-Jen; Lin, Hung-Hung; Wu, Pei-Chen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-06 |
Detection of a balanced homologous acrocentric rearrangement rea(14q14q) and low-grade X-chromosome mosaicism in a couple with repeated pregnancy losses |
陳持平; Chen, Chih-Ping; Chern, Schu-Rern; Wu, Chia-Hsun; Tsai, Fuu-Jen; Wu, Pei-Chen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-06 |
Fetal magnetic resonance imaging demonstration of central nervous system abnormalities and polydactyly associated with Joubert syndrome |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Huang, Jon-Kway; Liu, Yu-Peng; Tsai, Fuu-Jen; Yang, Chun-Kuang; Huang, Jian-Pei; Chen, Chen-Yu; Wu, Pei-Chen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-06 |
Mosaic tetrasomy 12p with discrepancy between fetal tissues and extraembryonic tissues: molecular analysis and possible mechanism of formation |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Chern, Schu-Rern; Tsai, Fuu-Jen; Wu, Pei-Chen; Chen, Hsaio-En Cindy; Chiang, Shu-Shien; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-06 |
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18 |
陳持平; Chen, Chih-Ping; Lin, Chyi-Chyang; Su, Yi-Ning; Tsai, Fuu-Jen; Chen, Yu-Ting; Chern, Schu-Rern; Lee, Chen-Chi; Town, Dai-Dyi; Chen, Li-Feng; Wu, Pei-Chen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-03 |
Abnormally flat facial profile on two- and three-dimensional ultrasound and array comparative genomic hybridization for the diagnosis of Pallister-Killian syndrome |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Hsu, Chin-Yuan; Tsai, Fuu-Jen; Chien, Shu-Chin; Chern, Schu-Rern; Lee, Meng-Shan; Wu, Pei-Chen; Chen, Hsaio-En Cindy; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-03 |
Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21->q11.23 by array comparative genomic hybridization |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Chern, Schu-Rern; Tsai, Fuu-Jen; Hsu, Chin-Yuan; Lee, Chen-Chi; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-03 |
Rapid genome-wide aneuploidy diagnosis using uncultured amniocytes and array CGH in pregnancy with abnormal ultrasound findings detected in late second and third trimesters |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Tsai, Fuu-Jen; Chern, Schu-Rern; Hsu, Chin-Yuan; Huang, Ming-Chao; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-03 |
Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following sonographic findings of mild ventriculomegaly and clenched hands mimicking trisomy 18 |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Hsu, Chin-Yuan; Ling, Pei-Ying; Tsai, Fuu-Jen; Chern, Schu-Rern; Wu, Pei-Chen; Chen, Hsaio-En Cindy; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-03 |
Unbalanced and balanced heterologous Robertsonian translocations involving chromosome 21 at amniocentesis |
陳持平; Chen, Chih-Ping; Chern, Schu-Rern; Wu, Pei-Chen; Tsai, Fuu-Jen; Lee, Chen-Chi; Town, Dai-Dyi; Chen, Wen-Lin; Chen, Li-Feng; Lee, Meng-Shan; Pan, Chen-Wen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2010-02 |
Prenatal diagnosis of X-linked myotubular myopathy |
陳持平; Chen, Chih-Ping; Lin, Shuan-Pei; Chern, Schu-Rern; Tsai, Fuu-Jen; Wang, Tao-Yeuan; Lin, Hung-Hung; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2009-12 |
Down syndrome due to unbalanced homologous acrocentric rearrangements and its recurrence in subsequent pregnancies: prenatal diagnosis by amniocentesis |
陳持平; Chen, Chih-Ping; Chern, Schu-Rern; Tsai, Fuu-Jen; Wu, Pei-Chen; Lee, Chen-Chi; Chiang, Shu-Shien; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2009-12 |
Limb-body wall complex in one fetus of a dizygotic twin pregnancy obtained by egg donation, in vitro fertilization and embryo transfer: prenatal diagnosis and literature review |
陳持平; Chen, Chih-Ping; Lee, Maw-Shuan; Tsai, Fuu-Jen; Huang, Ming-Chao; Chern, Schu-Rern; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2009-12 |
Prenatal diagnosis of a 22q11.2 microdeletion in a fetus with double-outlet right ventricle, pulmonary stenosis and a ventricular septal defect by array comparative genomic hybridization |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Chang, Tung-Yao; Chern, Schu-Rern; Tsai, Fuu-Jen; Hwang, Jonathan Kwei; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2009-12 |
Prenatal diagnosis of monosomy 17p (17p13.3->pter) associated with polyhydramnios, intrauterine growth restriction, ventriculomegaly and Miller-Dieker lissencephaly syndrome in a fetus |
; Lin, Chin-Yi; 陳持平; Chen, Chih-Ping; Liau, Chiung-Ling; Su, Pen-Hua; Tsao, Teng-Fu; Chang, Tung-Yao; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2009-12 |
Prenatal diagnosis of terminal 2q deletion and distal 15q duplication by array comparative genomic hybridization using uncultured amniocytes |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Tsai, Fuu-Jen; Lin, Hung-Hung; Chern, Schu-Rern; Lee, Meng-Shan; Hwang, Jonathan Kwei; Chen, Teresa Hsiao-Tien; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2009-12 |
Trisomy 13 mosaicism associated with cyclopia and cystic hygroma |
陳持平; Chen, Chih-Ping; Chern, Schu-Rern; Tsai, Fuu-Jen; Wu, Pei-Chen; Lee, Chen-Chi; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2009-12 |
Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis |
陳持平; Chen, Chih-Ping; Chern, Schu-Rern; Wu, Pei-Chen; Tsai, Fuu-Jen; Lee, Chen-Chi; Town, Dai-Dyi; Chen, Wen-Lin; Chen, Li-Feng; Lee, Meng-Shan; Pan, Chen-Wen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2009-09 |
Concomitant craniorachischisis and omphalocele in a male fetus: prenatal magnetic resonance imaging findings and literature review |
陳持平; Chen, Chih-Ping; Liu, Yu-Peng; Tsai, Fuu-Jen; Chen, Chen-Yu; Lin, Hung-Hung; Wu, Pei-Chen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2009-09 |
Prenatal diagnosis and molecular analysis of triploidy in a fetus with intrauterine growth restriction, relative macrocephaly and holoprosencephaly |
陳持平; Chen, Chih-Ping; Chern, Schu-Rern; Tsai, Fuu-Jen; Hsu, Chin-Yuan; Ko, Kevin; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2009-09 |
Prenatal diagnosis and molecular analysis of trisomy 13 mosaicism |
陳持平; Chen, Chih-Ping; Chern, Schu-Rern; Tsai, Fuu-Jen; Lin, Hung-Hung; Pan, Chen-Wen; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2009-09 |
Prenatal magnetic resonance imaging, ultrasound imaging findings and genetic analysis of concomitant rhabdomyomas and cerebral tuberous sclerosis |
陳持平; Chen, Chih-Ping; Su, Yi-Ning; Chang, Tung-Yao; Liu, Yu-Peng; Tsai, Fuu-Jen; Hwang, Jonathan Kwei; Wang, Wayseen |
|
| [生物科技學系] 期刊論文 |
2009-03 |
PRENATAL DIAGNOSIS OF 46,XX,DER(13;21)(Q10;Q10),+21 AND TRANSIENT ABNORMAL MYELOPOIESIS IN A FETUS WITH HEPATOSPLENOMEGALY AND SPONTANEOUS RESOLUTION OF FETAL ASCITES |
陳持平; Chen, Chih-Ping; Tsai, Fuu-Jen; Chern, Schu-Rern; Chang, Tung-Yao; Hsu, Chin-Yuan; Lin, Hung-Hung; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2009-01 |
A 12 Mb deletion of 6p24.1 -> pter in an 18-gestational-week fetus with orofacial clefting, the Dandy-Walker malformation and bilateral multicystic kidneys |
陳持平; Chen, Chih-Ping; Tzen, Chin-Yuan; Chern, Schu-Rern; Tsai, Fuu-Jen; Hsu, Chin-Yuan; Lee, Chen-Chi; Lee, Meng-Shan; Pan, Chen-Wen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2008-12 |
CONCOMITANT EXENCEPHALY AND LIMB DEFECTS ASSOCIATED WITH PENTALOGY OF CANTRELL |
陳持平; Chen, Chih-Ping; Tzen, Chin-Yuan; Chen, Chen-Yu; Tsai, Fuu-Jen; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2008-12 |
LIMB-BODY WALL COMPLEX WITH CRANIOFACIAL DEFECTS AFTER OVARIAN STIMULATION |
陳持平; Chen, Chih-Ping; Tsai, Fuu-Jen; Chen, Chen-Yu; Lin, Hung-Hung; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2008-10 |
Prenatal Diagnosis of Partial Trisomy 3p (3p21 -> pter) and Partial Monosomy 11q (11q23 -> qter) Associated with Abnormal Sonographic Findings of Holoprosencephaly, Orofacial Clefts, Pyelectasis and a Unilateral Duplex Renal System |
陳持平; Chen, Chih-Ping; Wang, Tzu-Hao; Lin, Chyi-Chyang; Tsai, Fuu-Jen; Hsieh, Lie-Jiau; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2008-03 |
CONCOMITANT OMPHALOCELE AND ANENCEPHALY ASSOCIATED WITH TRISOMY 18 AND ARTHROGRYPOSIS DIAGNOSED IN EARLY PREGNANCY |
陳持平; Chen, Chih-Ping; Chang, Tung-Yao; Lin, Hung-Hung; Chern, Schu-Rern; Wang, Wayseen |
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| [生物科技學系] 期刊論文 |
2008-03 |
PRENATAL VISUALIZATION OF CEBOCEPHALY WITH A PROMINENT NOSE IN A SECOND-TRIMESTER FETUS WITH ALOBAR HOLOPROSENCEPHALY AND TRISOMY 13 |
陳持平; Chen, Chih-Ping; Shih, Jin-Chung; Tzen, Chin-Yuan; Chern, Schu-Rern; Lin, Chen-Ju; Wang, Wayseen |
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| [生物資訊與醫學工程學系 ] 期刊論文 |
2016-12 |
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability |
陳持平; Chen, Chih-Ping; *; Li, Shuan-Pei; Lin, Shuan-Pei; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Ya, Chien-Wen; Yang, Chien-Wen; Le, Meng-Shan; Lee, Meng-Shan; Wang, Wayseen; Wang, Wayseen |
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| [醫學檢驗暨生物技術學系] 期刊論文 |
2019-11 |
Prenatal diagnosis of mosaicism for trisomy 7 in a single colony at amniocentesis in a pregnancy with a favorable outcome |
陳持平; Chen, Chih-Ping; Hung, Fang-Yu; Hung, Fang-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; Wu, Fang-Tzu; Wu, Fang-Tzu; Town, Dai-Dyi; Town, Dai-Dyi; Wang, Wayseen; Wang, Wayseen |
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| [醫學檢驗暨生物技術學系] 期刊論文 |
2019-11 |
Mosaic isochromosome 20q at amniocentesis: prenatal diagnosis, genetic counseling and literature review |
陳持平; Chen, Chih-Ping; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; Wu, Fang-Tzu; Wu, Fang-Tzu; Town, Dai-Dyi; Town, Dai-Dyi; Wang, Wayseen; Wang, Wayseen |
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| [醫學檢驗暨生物技術學系] 期刊論文 |
2019-11 |
Detection of a familial 1q21.1 microdeletion and concomitant CHD1L mutation in a fetus with oligohydramnios and bilateral renal dysplasia on prenatal ultrasound |
陳持平; Chen, Chih-Ping; Hua, Jian-Pei; Huang, Jian-Pei; Chen, Yi-Yung; Chen, Yi-Yung; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; Wang, Wayseen; Wang, Wayseen; Lee, Chen-Chi; Lee, Chen-Chi |
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| [醫學檢驗暨生物技術學系] 期刊論文 |
2019-11 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3 |
陳持平; Chen, Chih-Ping; Tsang-Ming, K; Ko, Tsang-Ming; Chen, Chen-Yu; Chen, Chen-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; Wu, Fang-Tzu; Wu, Fang-Tzu; Pan, Chen-Wen; Pan, Chen-Wen; Wang, Wayseen; Wang, Wayseen |
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| [醫學檢驗暨生物技術學系] 期刊論文 |
2019-11 |
Detection of a familial 21q22.3 microduplication in a fetus associated with congenital heart defects |
陳持平; Chen, Chih-Ping; Chen, Chen-Yu; Chen, Chen-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; Chua, Tzu-Yun; Chuang, Tzu-Yun; Wang, Wayseen; Wang, Wayseen |
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| [醫學檢驗暨生物技術學系] 期刊論文 |
2019-09 |
Mosaic trisomy 22 at amniocentesis: prenatal diagnosis and literature review |
陳持平; Chen, Chih-Ping; Hu, Ming-Chao; Huang, Ming-Chao; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; Chua, Tzu-Yun; Chuang, Tzu-Yun; Town, Dai-Dyi; Town, Dai-Dyi; Wang, Wayseen; Wang, Wayseen |
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| [醫學檢驗暨生物技術學系] 期刊論文 |
2019-09 |
Inv dup del(10p): prenatal diagnosis and molecular cytogenetic characterization |
陳持平; Chen, Chih-Ping; Tsang-Ming, K; Ko, Tsang-Ming; Wa, Liang-Kai; Wang, Liang-Kai; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; Wu, Fang-Tzu; Wu, Fang-Tzu; Chen, Li-Feng; Chen, Li-Feng; Wang, Wayseen; Wang, Wayseen |
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| [醫學檢驗暨生物技術學系] 期刊論文 |
2019-09 |
Detection of de novo del(18)(q22.2) and a familial of 15q13.2-q13.3 microduplication in a fetus with congenital heart defects |
陳持平; Chen, Chih-Ping; Chen, Chen-Yu; Chen, Chen-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; Wu, Fang-Tzu; Wu, Fang-Tzu; Chen, Li-Feng; Chen, Li-Feng; Wang, Wayseen; Wang, Wayseen |
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