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Showing items 41-65 of 68 (3 Page(s) Totally)
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Institution	Date	Title	Author
中國醫藥大學	2010-12	Ellis-van Creveld syndrome: prenatal diagnosis, molecular analysis and genetic counseling	陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Chin-Yuan Hsu); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Po-Tsang Chen); (Wayseen Wang)
中國醫藥大學	2010-09	Prenatal diagnosis of satellited 21q derived from pericentric inversion involving the satellite stalk region and terminal 21q	陳持平(Chih-Ping Chen)*; 蔡輔仁(Fuu-Jen Tsai); (Chen-Chi Lee); (Wen-Lin Chen); (Chen-Wen Pan); (Pei-Chen Wu); (Wayseen Wang)
中國醫藥大學	2010-09	A de novo 7.9 Mb deletion in 22q13.2->qter in a boy with autistic features, epilepsy, developmental delay atopic dermatitis and abnormal immunological findings	陳持平(Chih-Ping Chen)*; (Shuan-Pei Li); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Yu-Ting Chen); (Wayseen Wang)
中國醫藥大學	2010-09	Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3->pter) and partial monosomy 13q (13q33.3->qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly	陳持平(Chih-Ping Chen)*; (Ming Chen); (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Chin-Yuan Hsu); (Pei-Chen Wu); (Dai-Dyi Town); (Dong-Jay Lee); (Gwo-Chin Ma); (Wayseen Wang)
中國醫藥大學	2010-09	Mosaic ring chromosome 18, ring chromosome 18 duplication/deletion and disomy 18: perinatal findings and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization	陳持平(Chih-Ping Chen)*; (Yung-Ting Guo); (Shuan-Pei Lin); (Yi-Ning Su); (Yann-Jang Chen); (Rui-Yuan Hseuh); (Yi-Hui Lin); (Pei-Chen Wu); (Chen-Chi Lee); (Yu-Ting Chen); (Wayseen Wang)
中國醫藥大學	2010-09	Mosaic trisomy 7 at amniocentesis: prenatal diagnosis and molecular genetic analyses	陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Schu-Rern Chern); (Yu-Ming Hwu); (Shuan-Pei Lin); (Chyong-Hsin Hsu); 蔡輔仁(Fuu-Jen Tsai); (Tao-Yeuan Wang); (Pei-Chen Wu); (Chen-Chi Lee); (Yu-Ting Chen); (Li-Feng Chen); (Wayseen Wang)
中國醫藥大學	2010-09	Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses	陳持平(Chih-Ping Chen)*; (Hsien-Ming Lin); (Yi-Ning Su); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Yu-Ting Chen); (Meng-Shan Lee); (Chen-Wen Pan); (Wayseen Wang)
中國醫藥大學	2010-09	Prenatal diagnosis of persistent cloaca with hydrometrocolpos and ascites by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy	陳持平(Chih-Ping Chen)*; (Yu-Peng Liu); (Tung-Yao Chang); 蔡輔仁(Fuu-Jen Tsai); (Chen-Yu Chen); (Pei-Chen Wu); (Teresa Hsiao-Tien Chen); (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)
中國醫藥大學	2010-09	Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 22	陳持平(Chih-Ping Chen)*; (Chyi-Chyang Lin); (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Chen-Chi Lee); (Wen-Ling Chen); (Li-Feng Chen); (Pei-Chen Wu); (Wayseen Wang)
國立高雄師範大學	2010-08-16	高雄市政府公職人員英語學習動機、態度及需求之研究	吳佩蓁; Pei-Chen Wu
中國醫藥大學	2010-07	Array-CGH detection of a de novo 2.8 Mb deletion in 2q24.2/q24.3 in a girl with autistic features and developmental delay	陳持平(Chih-Ping Chen)*; (Shuan-Pei Lin); (Schu-Rern Chern); (Yann-Jang Chen); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Wayseen Wang)
中國醫藥大學	2010-06	Deletion 2q37.3->qter and duplication 15q24.3->qter characterized by array CGH in a girl with epilepsy and dysmorphic features	陳持平(Chih-Ping Chen)*; (Shuan-Pei Lin); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Li-Feng Chen); (Meng-Shan Lee); (Wayseen Wang)
中國醫藥大學	2010-06	Apert syndrome associated with upper airway obstruction and gastroesophageal reflux presenting polyhydramnios in the third trimester	陳持平(Chih-Ping Chen)*; (Shuan-Pei Lin); (Yi-Ning Su); (Chen-Yu Chen); 蔡輔仁(Fuu-Jen Tsai); (Yu-Peng Liu); (Schu-Rern Chern); (Pei-Chen Wu); (Hsaio-En Cindy Chen); (Wayseen Wang)
中國醫藥大學	2010-06	Detection of a balanced homologous acrocentric rearrangement rea(14q14q) and low-grade X-chromosome mosaicism in a couple with repeated pregnancy losses	陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); (Chia-Hsun Wu); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Wayseen Wang)
中國醫藥大學	2010-06	Detection and comparison of the levels of cytomegalovirus DNA in amniotic fluid and fetal ascites in a second-trimester fetus with massive ascites, hyperechogenic bowel, ventriculomegaly and intrauterine growth restriction	陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); (Tao-Yeuan Wang); 蔡輔仁(Fuu-Jen Tsai); (Hung-Hung Lin); (Pei-Chen Wu); (Wayseen Wang)
中國醫藥大學	2010-06	Mosaic tetrasomy 12p with discrepancy between fetal tissues and extraembryonic tissues: molecular analysis and possible mechanism of formation	陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Hsaio-En Cindy Chen); (Shu-Shien Chiang); (Wayseen Wang)
中國醫藥大學	2010-06	Fetal magnetic resonance imaging demonstration of central nervous system abnormalities and polydactyly associated with Joubert syndrome	陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Jon-Kway Huang); (Yu-Peng Liu); 蔡輔仁(Fuu-Jen Tsai); (Chun-Kuang Yang); (Jian-Pei Huang); (Chen-Yu Chen); (Pei-Chen Wu); (Wayseen Wang)
中國醫藥大學	2010-03	Second-trimester molecular prenatal diagnosis of sporadic Apert syndrome following sonographic findings of mild ventriculomegaly and clenched hands mimicking trisomy 18	陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Chin-Yuan Hsu); (Pei-Ying Ling); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Pei-Chen Wu); (Hsaio-En Cindy Chen); (Wayseen Wang)
中國醫藥大學	2010-03	UNBALANCED AND BALANCED HETEROLOGOUS ACROCENTRIC REARRANGEMENTS INVOLVING CHROMOSOME 21 AT AMNIOCENTESIS	陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); (Pei-Chen Wu); 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	2010-02	Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 18 and associated with a reciprocal translocation involving chromosomes 17 and 18	陳持平(Chih-Ping Chen)*; (Chyi-Chyang Lin); (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Yu-Ting Chen); (Schu-Rern Chern); (Chen-Chi Lee); (Dai-Dyi Town); (Li-Feng Chen); (Pei-Chen Wu); (Wayseen Wang)
中國醫藥大學	2009-12	Trisomy 13 mosaicism associated with cyclopia and cystic hygroma	陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Wayseen Wang)
中國醫藥大學	2009-12	Down syndrome due to unbalanced homologous acrocentric rearrangements and its recurrence in subsequent pregnancies: prenatal diagnosis by amniocentesis	陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Shu-Shien Chiang); (Wayseen Wang)
中國醫藥大學	2009-12	Unbalanced and balanced acrocentric rearrangements involving chromosomes other than chromosome 21 at amniocentesis	陳持平(Chih-Ping Chen)*; (Schu-Rern Chern); (Pei-Chen Wu); 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	2009-09	Concomitant craniorachischisis and omphalocele in a male fetus: prenatal magnetic resonance imaging findings and literature review	陳持平(Chih-Ping Chen)*; (Yu-Peng Liu); 蔡輔仁(Fuu-Jen Tsai); (Chen-Yu Chen); (Hung-Hung Lin); (Pei-Chen Wu); (Wayseen Wang)

Showing items 41-65 of 68 (3 Page(s) Totally)
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