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Taiwan Academic Institutional Repository >
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"陳持平"
Showing items 6-15 of 339 (34 Page(s) Totally)
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| 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 |
| 亞洲大學 |
2019-09 |
Mosaic trisomy 22 at amniocentesis: prenatal diagnosis and literature review
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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 |
| 亞洲大學 |
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
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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;Wu, Fang-Tzu;Wu, Fang-Tzu;Chen, Li-Feng;Chen, Li-Feng;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2019-09 |
Inv dup del(10p): prenatal diagnosis and molecular cytogenetic characterization
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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 |
| 亞洲大學 |
2018-10 |
Detection of hypomethylation of H19 in a pregnancy with limb-body wall complex
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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 |
| 亞洲大學 |
2018-10 |
First-trimester cystic hygroma and omphalocele in a fetus with Turner syndrome
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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 |
| 亞洲大學 |
2018-10 |
Prenatal diagnosis of a familial 15q11.2 (BP1-BP2) microdeletion encompassing TUBGCP5, CYFIP1, NIPA2 and NIPA1 in a fetus with ventriculomegaly, microcephaly and intrauterine growth restriction on prenatal ultrasound
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陳持平;Chen, Chih-Ping;Cha, Shu-Yuan;Chang, Shu-Yuan;Wa, Liang-Kai;Wang, Liang-Kai;Cha, Tung-Yao;Chang, Tung-Yao;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, hin-Wen;Chen, hin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Ya, Chien-Wen;Yang, Chien-Wen |
| 亞洲大學 |
2018-10 |
Prenatal diagnosis of a familial 1q21.1-q21.2 microdeletion in a fetus with polydactyly of left foot on prenatal ultrasound
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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 |
Showing items 6-15 of 339 (34 Page(s) Totally)
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