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Items for Author "Huang, Jian-Pei"
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Showing 8 items.
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Collection |
Date |
Title |
Authors |
Bitstream |
| [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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| [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 |
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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 |
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 |
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 |
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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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