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機構	日期	題名	作者
中國醫藥大學	2011-09	Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization and perinatal findings in a fetus with dup(15)(q26.2q26.3)	陳持平(Chih-Ping Chen)*;(Yi-Hui Lin);(Heng-Kien Au);(Chin-Yuan Hsu);(Yu-Peng Liu);(Pei-Chen Wu);(Schu-Rern Chern);(Yu-Ting Chen);(Li-Feng Chen);(Adam Hwa-Ming Hsieh);(Wayseen Wang)
中國醫藥大學	2011-09	Prenatal diagnosis of microvillus inclusion disease	陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Schu-Rern Chern);(Pei-Chen Wu);(Wayseen Wang)
亞洲大學	2011-06	Prenatal diagnosis and array comparative genomic hybridization characterization of a de novo interstitial deletion of chromosome 20p	陳持平;Chen, Chih-Ping;Yi-Ning Su;Schu-Rern Chern;Fuu-Jen Tsai;Pei-Chen Wu;Chen-Chi Lee;Wayseen Wang
中國醫藥大學	2011-06	Rapid aneuploidy diagnosis by array comparative genomic hybridization using uncultured amniocytes in a pregnancy with fetal nuchal edema and mild ascites	陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Pei-Chen Wu);(Chen-Chi Lee);(Chen-Wen Pan);(Wayseen Wang)
中國醫藥大學	2011-06	Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic isochromosome 20q detected at amniocentesis	陳持平(Chih-Ping Chen)*;(Jui-Der Liou);(Chi-Hsin Chiang);(Yi-Ning Su);(Schu-Rern Chern);蔡輔仁(Fuu-Jen Tsai);(Pei-Chen Wu);(Yu-Ting Chen);(Chen-Chi Lee);(Wen-Lin Chen);(Wayseen Wang)
中國醫藥大學	2011-06	Prenatal diagnosis of cerebral tubers by magnetic resonance imaging following detection of cardiac rhabdomyomas by prenatal ultrasound in a fetus with a nonsense mutation in the TSC2 gene	陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Chin-Yuan Hsu);(Ming-Ren Chen);(Yu-Peng Liu);(Pei-Chen Wu);(Wayseen Wang)
中國醫藥大學	2011-03	Unbalanced reciprocal translocations at amniocentesis	陳持平(Chih-Ping Chen)*; (Pei-Chen Wu); (Schu-Rern Chern); 蔡輔仁(Fuu-Jen Tsai); (Dai-Dyi Town); (Wen-Lin Chen); (Li-Feng Chen); (Meng-Shan Lee); (Chen-Wen Pan); (Wayseen Wang)
中國醫藥大學	2011-03	Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization	陳持平(Chih-Ping Chen)*; (Yi-Ning Su); (Schu-Rern Chern); (Chin-Yuan Hsu); 蔡輔仁(Fuu-Jen Tsai); (Pei-Chen Wu); (Chen-Chi Lee); (Yu-Ting Chen); (Meng-Shan Lee); (Wayseen Wang)
中國醫藥大學	2011-03	Pathological characterization of a malformed umbilical cord associated with body stalk anomaly	陳持平(Chih-Ping Chen)*; (Tao-Yeuan Wang); (Pei-Chen Wu); 蔡輔仁(Fuu-Jen Tsai); (Wayseen Wang)
中國醫藥大學	2011-03	Congenital tracheal stenosis in a boy with the 22q13.3 deletion syndrome	陳持平(Chih-Ping Chen)*; (Shuan-Pei Lin); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Pei-Chen Wu); (Chen-Chi Lee); (Meng-Shan Lee); (Yu-Ting Chen); (Wayseen Wang)
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)
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)

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