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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
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Showing items 116-125 of 253  (26 Page(s) Totally)
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Institution Date Title Author
國立臺灣大學 2010 Mosaic Trisomy 7 at Amniocentesis: Prenatal Diagnosis and Molecular Genetic Analyses 陳持平; 蘇怡寧; 陳樹人; 林炫沛; 許瓊心; 蔡輔仁; 王道遠; 吳佩臻; 李貞姫; 陳麗鳳; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHERN, SCHU-RERN; LIN, SHUAN-PEI; HSU, CHYONG-HSIN; TSAI, FUU-JEN; WANG, TAO-YEUAN; WU, PEI-CHEN; LEE, CHEN-CHI; CHEN, LI-FENG; WANG, WAYSEEN
國立臺灣大學 2010 Mosaic Trisomy 9 at Amniocentesis: Prenatal Diagnosis and Molecular Genetic Analyses 陳持平; 蘇怡寧; 陳樹人; 蔡輔仁; 吳佩臻; 李貞姫; 李孟珊; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; WU, PEI-CHEN; LEE, CHEN-CHI; LEE, MENG-SHAN; WANG, WAYSEEN
國立臺灣大學 2010 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; 林齊强; 蘇怡寧; 蔡輔仁; 陳樹人; 李貞姫; 吳佩臻; 王偉信; CHEN, CHIH-PING; LIN, CHYI-CHYANG; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; LEE, CHEN-CHI; WU, PEI-CHEN; WANG, WAYSEEN
國立臺灣大學 2010 Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived from Chromosome 22 陳持平; 林齊强; 蘇怡寧; 蔡輔仁; 陳樹人; 李貞姫; 吳佩臻; 王偉信; CHEN, CHIH-PING; LIN, CHYI-CHYANG; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; LEE, CHEN-CHI; WU, PEI-CHEN; WANG, WAYSEEN
國立臺灣大學 2010 Prenatal Diagnosis of a 4.9-Mb Deletion of 10q11.21 -> Q11.23 by Array Comparative Genomic Hybridization 陳持平; 蘇怡寧; 陳樹人; 蔡輔仁; 徐金源; 李貞姫; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHERN, SCHU-RERN; TSAI, FUU-JEN; HSU, CHIN-YUAN; LEE, CHEN-CHI; WANG, WAYSEEN
國立臺灣大學 2010 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; 蘇怡寧; 張東曜; 劉育朋; 蔡輔仁; 陳銘仁; 王偉信; CHEN, CHIH-PING; SU, YI-NING; CHANG, TUNG-YAO; LIU, YU-PENG; TSAI, FUU-JEN; CHEN, MING-REN; WANG, WAYSEEN
國立臺灣大學 2010 Rapid Genome-Wide Aneuploidy Diagnosis Using Uncultured Amniocytes and Array Comparative Genomic Hybridization in Pregnancy with Abnormal Ultrasound Findings Detected in Late Second and Third Trimesters 陳持平; 蘇怡寧; 蔡輔仁; 陳樹人; 徐金源; 黃閔照; 王偉信; CHEN, CHIH-PING; SU, YI-NING; TSAI, FUU-JEN; CHERN, SCHU-RERN; HSU, CHIN-YUAN; HUANG, MING-CHAO; WANG, WAYSEEN
國立臺灣大學 2010 Second-Trimester Molecular Prenatal Diagnosis of Sporadic Apert Syndrome Following Sonographic Findings of Mild Ventriculomegaly and Clenched Hands Mimicking Trisomy 18 陳持平; 蘇怡寧; 徐金源; 蔡輔仁; 陳樹人; 吳佩臻; 王偉信; 林珮瑩; CHEN, CHIH-PING; SU, YI-NING; HSU, CHIN-YUAN; TSAI, FUU-JEN; CHERN, SCHU-RERN; WU, PEI-CHEN; WANG, WAYSEEN; LING, PEI-YING
國立臺灣大學 2010 Novel Neurotrophic Tyrosine Kinase Receptor Type 1 Gene Mutation Associated with Congenital Insensitivity to Pain with Anhidrosis 林宜霈; 蘇怡寧; 翁妏謹; 李旺祚; LIN, YI-PEI; SU, YI-NING; WENG, WEN-CHIN; LEE, WANG-TSO
國立臺灣大學 2010 Phenotypic Analyses and Mutation Screening of the Slc26a4 and Foxi1 Genes in 101 Taiwanese Families with Bilateral Nonsyndromic Enlarged Vestibular Aqueduct (Dfnb4) or Pendred Syndrome 吳振吉; 呂盈璋; 陳培哲; 葉柏伶; 蘇怡寧; 胡務亮; 許權振; WU, CHEN-CHI; LU, YING-CHANG; CHEN, PEI-JER; YEH, PO-LIN; SU, YI-NING; HWU, WUH-LIANG; HSU, CHUAN-JEN

Showing items 116-125 of 253  (26 Page(s) Totally)
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