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機構 日期 題名 作者
中國醫藥大學 2011-03 Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations 陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Shin-Yu Lin); (Chih-Long Chang); (Yeou-Lih Wang); (Jiau-Pei Huang); (Chen-Yu Chen); (Fang-Yu Hung); (Yi-Yung Chen); (Pei-Chen Wu); (Wayseen Wang)
亞洲大學 2010-12 Ellis-van Creveld syndrome: prenatal diagnosis, molecular analysis and genetic counseling Chih-Ping Chen; Yi-Ning Su;Chin-Yuan Hsu;Schu-Rern Chern;Fuu-Jen Tsai;Pei-Chen Wu;Po-Tsang Chen;Wayseen Wang
中國醫藥大學 2010-12 Prenatal diagnosis of partial monosomy 1q (1q42.3->qter) associated with hydrocephalus and corpus callosum agenesis 陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Hung-Hung Lin); (Pei-Chen Wu); (Chen-Chi Lee); (Chen-Wen Pan); (Wayseen Wang)
中國醫藥大學 2010-12 A 5.3-Mb duplication of 9p12->p13.1 characterized by array CGH in a female infant with developmental delay 陳持平(Chih-Ping Chen)*; (Shuan-Pei Lin); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chen-Chi Lee); (Chen-Wen Pan); (Pei-Chen Wu); (Wayseen Wang)
中國醫藥大學 2010-12 Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings 陳持平(Chih-Ping Chen)*; (Ming Chen); (Yi-Ning Su); (Chin-Yuan Hsu); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Pei-Chen Wu); (Chen-Chi Lee); (Wayseen Wang)
中國醫藥大學 2010-12 Balanced reciprocal translocations at amniocentesis 陳持平(Chih-Ping Chen)*; (Pei-Chen Wu); (Yi-Ning Su); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chen-Chi Lee); (Dai-Dyi Town); (Wen-Lin Chen); (Li-Feng Chen); (Meng-Shan Lee); (Chen-Wen Pan); (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 2010-12 Partial trisomy 16p (16p12.2->pter) and partial monosomy 22q (22q13.31->qter) presenting with fetal ascites and ventriculomegaly: prenatal diagnosis and array comparative genomic hybridization characterization 陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Richard Shih-Hung Young); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Schu-Rern Chern); (Dai-Dyi Town); (Chen-Wen Pan); (Wayseen Wang)
中國醫藥大學 2010-12 Partial trisomy 10q (10q25.1->qter) and partial monosomy 13q (13q34->qter) presenting with fetal pyelectasis: prenatal diagnosis and array comparative genomic hybridization characterization 陳持平(Chih-Ping Chen)*; (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Chin-Yuan Hsu); (Schu-Rern Chern); (Pei-Chen Wu); (Chen-Chi Lee); (Wen-Lin Chen); (Wayseen Wang)
中國醫藥大學 2010-12 Recurrent distal 16q duplication and terminal 22q deletion: prenatal diagnosis and genetic counseling 陳持平(Chih-Ping Chen)*; (Ming-Chao Huang); (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Dai-Dyi Town); (Chen-Wen Pan); (Wayseen Wang)

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