臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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"陳持平 chih ping chen"

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Showing items 101-110 of 255 (26 Page(s) Totally)
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Institution	Date	Title	Author
中國醫藥大學	2012-03	Prenatal ultraousnd and magnetic resonance imaging findings of fetal akinesia deformation sequence with multiple pterygium syndrome	陳持平(Chih-Ping Chen)*;(Jin-Chung Shih);(Chen-Yu Chen);(Yu-Peng Liu);(Schu-Rern Chern);(Jun-Wei Su);(Wayseen Wang)
中國醫藥大學	2012-03	MUC2 polymorphisms are associated with endometriosis development and infertility: a case-control study	張穎宜(Yin-Yi Chang);(Yi Chen);林武周(Wu-Chou Lin);陳志玫(Chih-Mei Chen);陳持平(Chih-Ping Chen);李尚熾(Shan Chih Lee);許晉銓(Jinn-Chyuan Sheu);蔡輔仁(Fuu-Jen Tsai)
中國醫藥大學	2012-03	MUC2 polymorphisms are associated with endometriosis development and infertility: a case-control study	張穎宜(Yin-Yi Chang);(Yi Chen);林武周(Wu-Chou Lin);陳志玫(Chih-Mei Chen);陳持平(Chih-Ping Chen);李尚熾(Shan Chih Lee);許晉銓(Jinn-Chyuan Sheu);蔡輔仁(Fuu-Jen Tsai)
中國醫藥大學	2012-03	Rapid aneuploidy diagnosis of partial trisomy 7q (7q34->qter) and partial monosomy 10q (10q26.12->qter) by array comparative genomic hybridization using uncultured amniocytes	陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Yi-Ning Su);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Dai-Dyi Town);(Li-Feng Chen);(Meng-Shan Lee);(Wayseen Wang)
中國醫藥大學	2012-03	Prenatal diagnosis and genetic analysis of fetal akinesia deformation sequence and multiple pterygium syndrome associated with neuromuscular junction disorders: a review	陳持平(Chih-Ping Chen)*
中國醫藥大學	2012-03	Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification using uncultured amniocytes in pregnancy with major fetal structural abnormalities	陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Chih-Long Chang);(Yi-Yung Chen);(Jun-Wei Su);(Schu-Rern Chern);(Wayseen Wang)
中國醫藥大學	2011-12	Pure interstitial duplication of chromosome 7q (7q31.2->q33) in a 4-year-old girl with growth restriction, short stature, speech delay and mental retardation	陳持平(Chih-Ping Chen)*;(Shuan-Pei Lin);(Schu-Rern Chern);蔡輔仁(Fuu-Jen Tsai);(Meng-Shan Lee);(Yen-Jiun Chen);(Wayseen Wang)
中國醫藥大學	2011-12	Perinatal magnetic resonance imaging demonstration of duplication of the right renal collecting system with ipsilateral hydronephrosis and hydroureter, and contralateral renal hypoplasia	陳持平(Chih-Ping Chen)*;(Jeng-Daw Tsai);(Chin-Yuan Hsu);(Tung-Yao Chang);(Yu-Peng Liu);(Jun-Wei Su);(Wayseen Wang)
中國醫藥大學	2011-12	A de novo duplication of chromosome 21q22.11->qter associated with Down syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings	陳持平(Chih-Ping Chen)*;(Hsu-Kuaing Huang);(Pei-Ying Lin);(Yi-Ning Su);(Ming Chen);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Schu-Rern Chern);(Yu-Ting Chen);(Chen-Chi Lee);(Wayseen Wang)
中國醫藥大學	2011-12	Prenatal diagnosis of a de novo interstitial deletion of chromosome 20q12 in a fetus with complex congenital heart defects, corpus callosum agenesis and intrauterine growth restriction	(Yi-Hui Lin);陳持平(Chih-Ping Chen)*;(Tze-Chien Chen);(Chun-Sen Hsu);(Szu-Yuan Chou);簡淑錦(Shu-Chin Chien)

Showing items 101-110 of 255 (26 Page(s) Totally)
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