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    Items for Author "Che, Shin-Wen" 

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    Showing 49 items.

    Collection Date Title Authors Bitstream
    [生物科技學系] 期刊論文 2018-10 Prenatal diagnosis of a familial 5p14.3-p14.1 deletion encompassing CDH18, CDH12, PMCHL1, PRDM9 and CDH10 in a fetus with congenital heart disease on prenatal ultrasound 陳持平; Chen, Chih-Ping; Cha, Shu-Yuan; Chang, Shu-Yuan; Lin, Chen-Ju; Lin, Chen-Ju; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; Lai, hih-Ting; Lai, hih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Chen, Wen-Lin; Chen, Wen-Lin; Ya, Chien-Wen; Yang, Chien-Wen
    [生物科技學系] 期刊論文 2018-10 Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound 陳持平; Chen, Chih-Ping; Cha, Shu-Yuan; Chang, Shu-Yuan; Chen, Yen-Ni; Chen, Yen-Ni; 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; Chen, Li-Feng; Chen, Li-Feng
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [生物科技學系] 期刊論文 2016-12 Prenatal diagnosis of low-level mosaicism for trisomy 18 associated with a favorable fetal 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; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Le, Meng-Shan; Lee, Meng-Shan; Ya, Chien-Wen; Yang, Chien-Wen
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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
    [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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