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"wu peih shan"的相关文件
显示项目 1-10 / 79 (共8页)
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| 亞洲大學 |
2020-01-20 |
Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum
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Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; Wang, Wayseen; Ch, Chih-Ping; Chen, Chih-Ping; Hs, Chin-Yuan; Hsu, Chin-Yuan |
| 亞洲大學 |
2020-01-20 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis
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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 |
| 亞洲大學 |
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
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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 |
| 亞洲大學 |
2020-01-20 |
Prenatal diagnosis and molecular cytogenetic characterization of de novo distal 5p deletion and distal 22q duplication
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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 |
| 亞洲大學 |
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
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Chen, Chih-Ping; Lin, Yi-Hui; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Che, Shin-Wen; Chen, Shin-Wen; Wu, Fang-Tzu; Le, Meng-Shan; Lee, Meng-Shan; Chen, Yun-Yi; Wang, Wayseen; Ch, Chih-Ping |
| 亞洲大學 |
2019-11 |
Detection of a familial 21q22.3 microduplication in a fetus associated with congenital heart defects
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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 |
| 亞洲大學 |
2019-11 |
Mosaic isochromosome 20q at amniocentesis: prenatal diagnosis, genetic counseling and literature review
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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 |
| 亞洲大學 |
2019-11 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3
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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 |
| 亞洲大學 |
2019-11 |
Prenatal diagnosis of mosaicism for trisomy 7 in a single colony at amniocentesis in a pregnancy with a favorable outcome
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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 |
| 亞洲大學 |
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
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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 |
显示项目 1-10 / 79 (共8页)
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