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显示项目 146-170 / 213 (共9页)
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机构 日期 题名 作者
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 2010-12 Microvillus inclusion disease: prenatal ultrasound findings, molecular diagnosis and genetic counseling of congenital diarrhea 陳持平(Chih-Ping Chen)*; (Ming-Chou Chiang); (Tzu-Hao Wang); (Chuen Hsueh); (Shueen-Dyh Chang); 蔡輔仁(Fuu-Jen Tsai); (Chao-Ning Wang); (Schu-Rern Chern); (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 of rhabdomyomas and cerebral tuberous sclerosis by magnetic resonance imaging in one fetus of a dizygotic twin pregnancy associated with a frameshift mutation in the TSC2 gene 陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Tung-Yao Chang); (Yu-Peng Liu); 蔡輔仁(Fuu-Jen Tsai); (Ming-Ren Chen); (Jonathan Kwei Hwang); (Teresa Hsiao-Tien 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)
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)
亞洲大學 2010-03 Ventriculomegaly, intrauterine growth restriction and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2->pter) in a fetus Chih-Ping Chen;Yu-Peng Liu;Shaun-Pei Lin;Ming Chen;Fuu-Jen Tsai;Yu-Ting Chen;Li-Feng Chen;Jonathan Kwei Hwang;Wayseen Wang
中國醫藥大學 2010-03 Rapid genome-wide aneuploidy diagnosis using uncultured amniocytes and array CGH in pregnancy with abnormal ultrasound findings detected in late second and third trimesters 陳持平(Chih-Ping Chen)*; (Yi-Ning Su); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Chin-Yuan Hsu); (Ming-Chao Huang); (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 Prenatal diagnosis of a 4.9-Mb deletion of 10q11.21->q11.23 by array comparative genomic hybridization 陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Chin-Yuan Hsu); (Chen-Chi Lee); (Wayseen Wang)
中國醫藥大學 2010-03 Ventriculomegaly, intrauterine growth restriction and congenital heart defects as salient prenatal sonographic findings of Miller-Dieker lissencephaly syndrome associated with monosomy 17p (17p13.2->pter) in a fetus 陳持平(Chih-Ping Chen)*; (Yu-Peng Liu); (Shuan-Pei Lin); (Ming Chen); 蔡輔仁(Fuu-Jen Tsai); (Yu-Ting Chen); (Li-Feng Chen); (Jonathan Kwei Hwang); (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)

显示项目 146-170 / 213 (共9页)
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