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显示项目 1-10 / 59 (共6页)
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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 2020-01-20 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for r(13), monosomy 13 and idic r(13) by amniocentesis 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 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 2018-02 Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities 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;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Ya, Chien-Wen;Yang, Chien-Wen;Lee, Chen-Chi;Lee, Chen-Chi;Wang, Wayseen;Wang, Wayseen
亞洲大學 2018-02 Late-onset fetal bilateral pleural effusions associated with Down syndrome La, Shih-Ting;陳持平;Chen, Chih-Ping;*;Lin, Chen-Ju;Lin, Chen-Ju;Hs, Chin-Yuan;Hsu, Chin-Yuan;Wu, Peih-Shan;Wu, Peih-Shan;Lee, Chen-Chi;Lee, Chen-Chi;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen
亞洲大學 2017-12 Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1 陳持平;Chen, Chih-Ping;Hs, Chih-Heng;Hsieh, Chih-Heng;Ch, Schu-Rern;Chern, Schu-Rern;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;Lee, Chen-Chi;Wang, Wayseen
亞洲大學 2017-12 Prenatal diagnosis of low-level mosaicism for trisomy 13 at amniocentesis associated with a favorable outcome 陳持平;Chen, Chih-Ping;Ch, Schu-Rern;Chern, Schu-Rern;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;Lee, Chen-Chi;Wang, Wayseen
亞洲大學 2017-12 Prenatal diagnosis of an 8q22.2-q23.3 deletion associated with bilateral cleft lip and palate and intrauterine growth restriction on fetal ultrasound 陳持平;Chen, Chih-Ping;Cha, Tung-Yao;Chang, Tung-Yao;Hung, Fang-Yu;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Lee, Chen-Chi;Wang, Wayseen
亞洲大學 2016-12 Prenatal diagnosis of low-level mosaicism for trisomy 12 associated with a favorable pregnancy outcome 陳持平;Chen, Chih-Ping;*;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Lee, Chen-Chi;Lee, Chen-Chi;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen

显示项目 1-10 / 59 (共6页)
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