Items for Author "Chen, Wen-Lin"
Return to Browse by Author
Showing 23 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 |
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 |
2018-08 |
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 |
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)(::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 |
|
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 |
|
| [生物科技學系] 期刊論文 |
|
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 |
|
| [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 |
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 |
|
| [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 |
|
| [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 |
|
| [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 |
|
| [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 |
|
| [生物科技學系] 期刊論文 |
2014-03 |
Chromosomal deletions detected at amniocentesis |
Lin, Chen-Ju; Lin, Chen-Ju; 陳持平; Chen, Chih-Ping; Chi, Shu-Chin; Chien, Shu-Chin; Lee, Chen-Chi; Chen-Chi Lee,; Town, Dai-Dyi; Town, Dai-Dyi; Chen, Wen-Lin; Chen, Wen-Lin; Che, L i-Feng; Chen, L i-Feng; Le, Meng-Shan; Lee, Meng-Shan; Chen-Wen Pan,; Ku-Chien Lin,; Yeh, Tze-Tien; Yeh, Tze-Tien |
|
| [生物科技學系] 期刊論文 |
|
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 |
|
| [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 |
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 |
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 |
2010-09 |
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 |
2010-03 |
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 |
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 |
|
|
