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机构 日期 题名 作者
亞洲大學 2022-09-01 Progressive increase of the mosaic level for 45,X in 45,X/46,XX at different amniocenteses and postnatal progressive decrease of the 45,X cell line in a mosaic 45,X/46,XX fetus with a favorable outcome 陳持平;Chen, Chih-Ping;Ch, Schu-Rern;Chern, Schu-Rern;Che, Shin-Wen;Chen, Shin-Wen;Wu, Fang-Tzu;Wu, Fang-Tzu;Lee, Chen-Chi;Lee, Chen-Chi;Chen, Wen-Lin;Chen, Wen-Lin;Chen, Yun-Yi;Chen, Yun-Yi;Wang, Wayseen;Wang, Wayseen
亞洲大學 2022-09-01 Detection of mosaicism for 46,X,i(Y)(q10) in the blood lymphocytes in a phenotypically normal male neonate with prenatally detected 45,X/46,XY at amniocentesis and cytogenetic discrepancy in various tissues 陳持平;Chen, Chih-Ping;Ch, Schu-Rern;Chern, Schu-Rern;Che, Shin-Wen;Chen, Shin-Wen;Wu, Fang-Tzu;Wu, Fang-Tzu;Lee, Chen-Chi;Lee, Chen-Chi;Chen, Wen-Lin;Chen, Wen-Lin;Chen, Yun-Yi;Chen, Yun-Yi;Wang, Wayseen;Wang, Wayseen
亞洲大學 2022-09-01 The significance of karyotyping and azoospermia factor analysis in patients with nonobstructive azoospermia or oligozoospermia Che, Shin-Wen;Chen, Shin-Wen;陳持平;Chen, Chih-Ping;Ch, Schu-Rern;Chern, Schu-Rern;Kuo, Yu-Ling;Kuo, Yu-Ling;Chien-Ling, Chien-Ling C;Chiu, Chien-Ling
亞洲大學 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
亞洲大學 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
亞洲大學 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
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 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 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 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 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

显示项目 1-10 / 339 (共34页)
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