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Showing items 1-10 of 17  (2 Page(s) Totally)
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Institution Date Title Author
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
臺大學術典藏 2022-03-14T23:45:39Z Prenatal diagnosis and molecular cytogenetic characterization of a familial small supernumerary marker chromosome derived from the acrocentric chromosome 14/22 Chen, Chih Ping; MING CHEN; Ma, Gwo Chin; Chang, Shun Ping; Chern, Schu Rern; Chen, Shin Wen; Wu, Fang Tzu; Chen, Wen Lin; Lee, Meng Shan; Chen, Yun Yi; Wang, Wayseen
臺大學術典藏 2022-01-15T00:08:30Z Molecular cytogenetic characterization of a de novo small supernumerary marker chromosome derived from chromosome 15 in a pregnancy with incidental detection of a maternal Robertsonian translocation of 45,XX,der(13;14) (q10;q10) Chen, Chih Ping; MING CHEN; Ma, Gwo Chin; Chang, Shun Ping; Chern, Schu Rern; Chen, Shin Wen; Wu, Fang Tzu; Lee, Meng Shan; 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 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 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 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 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

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