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Showing items 1-14 of 14  (1 Page(s) Totally)
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Institution Date Title Author
中國醫藥大學 2015-02 Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma 陳持平(Chih-Ping Chen)*;(Tsang-Ming Ko);(Ming-Chao Huang);(Schu-Rern Chern);(Tan-Wei Lin);(Tung-Yao Chang);(Yu-Ling Kuo);(Wen-Lin Chen);(Wayseen Wang)
中國醫藥大學 2014-12 First-trimester molecular diagnosis of complete hydatidiform mole associated with dizygotic twin pregnancy conceived by intrauterine insemination 陳持平(Chih-Ping Chen)*;(Tsang-Ming Ko);(Chen-Yu Chen);(Tao-Yeuan Wang);(Schu-Rern Chern);(Yu-Ling Kuo);(Wayseen Wang)
亞洲大學 2014-06 Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects Yu-Ling Kuo;Chih-Ping Chen;Liang-Kai Wang;Tsang-Ming Ko;Tung-Yao Chang;Schu-Rern Chern;Peih-Shan Wu;Yu-Ting Chen;Shu-Yuan Chang
中國醫藥大學 2014-06 Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects Yu-Ling Kuo;陳持平(Chih-Ping Chen)*;(Liang-Kai Wang);(Tsang-Ming Ko);(Tung-Yao Chang);(Schu-Rern Chern);(Peih-Shan Wu);(Yu-Ting Chen);(Shu-Yuan Chang)
亞洲大學 2014-03 Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid confirmation of low-level mosaicism for tetrasomy 18p Chih-Ping Chen;Chen-Li Lin;Tsang-Ming Ko;Schu-Rern Chern;Yu-Ting Chen;Peih-Shan Wu;Yu-Ling Kuo;Meng-Shan Lee;Wayseen Wang
中國醫藥大學 2014-03 Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid confirmation of low-level mosaicism for tetrasomy 18p 陳持平(Chih-Ping Chen)*;(Chen-Ju Lin);(Tsang-Ming Ko);(Schu-Rern Chern);(Yu-Ting Chen);(Peih-Shan Wu);(Yu-Ling Kuo);(Meng-Shan Lee);(Wayseen Wang)
亞洲大學 2013-03 Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2->q11.21) 陳持平;Chen, Chih-Ping;Tsang-Ming Ko;Yi-Ning Su;Jun-Wei Su;Yu-Ting Chen;Chen-Chi Lee;Li-Feng Chen;Wayseen Wang
中國醫藥大學 2013-03 Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2->q11.21) 陳持平(Chih-Ping Chen)*;(Tsang-Ming Ko);(Yi-Ning Su);(Jun-Wei Su);(Yu-Ting Chen);(Chen-Chi Lee);(Li-Feng Chen);(Wayseen Wang)
中國醫藥大學 2013-01 Array comparative genomic hybridization characterization of prenatally detected de novo apparently balanced reciprocal translocations with or without genomic imbalance in other chromosome 陳持平(Chih-Ping Chen)*;(Ming Chen);(Gwo-Chin Ma);(Yi-Ning Su);(Tsang-Ming Ko);(Yi-Hui Lin);(Wayseen Wang)
中國醫藥大學 2012-12 Prenatal diagnosis of mosaic tetrasomy 18p 陳持平(Chih-Ping Chen)*;(Tsang-Ming Ko);(Yi-Ning Su);(Schu-Rern Chern);(Jun-Wei Su);(Yu-Ting Chen);(Dai-Dyi Town);(Wayseen Wang)
中國醫藥大學 2012-03 Prenatal diagnosis of partial trisomy 16p (16p12.2->pter) and partial monosomy 22q (22q13.31->qter) associated with increased nuchal translucency and abnormal maternal serum biochemistry in the first trimester 陳持平(Chih-Ping Chen)*;(Tsang-Ming Ko);(Yi-Ning Su);(Chin-Yuan Hsu);(Yi-Yung Chen);(Jun-Wei Su);(Wen-Lin Chen);(Wayseen Wang)
中國醫藥大學 2010-12 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8 陳持平(Chih-Ping Chen)*; (Ming Chen); (Tsang-Ming Ko); (Gwo-Chin Ma); 蔡輔仁(Fuu-Jen Tsai); (Ming-Song Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Li-Feng Che); (Wayseen Wang)
中國醫藥大學 2010-09 Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21 陳持平(Chih-Ping Chen)*; (Chyi-Chyang Lin); (Tsang-Ming Ko); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Chen-Chi Lee); (Yu-Ting Chen); (Pei-Chen Wu); (Wayseen Wang)
國立臺灣大學 1992 Factors Affecting Womens Acceptance of Amniocentesis and Their Concerns Lian, Hwa Heang; Tsang, Ming Ko; Fon, Jou-Hsieh; 李鎡堯; Lian, Hwa Heang; Tsang, Ming Ko; Fon, Jou-Hsieh; Lee, Tzu-Yao

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