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

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	造訪人次 : 52808130 線上人數 : 579 教育部委託研究計畫計畫執行:國立臺灣大學圖書館

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

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	2019臺灣學術機構典藏研討會
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機構	日期	題名	作者
中國醫藥大學	2015-12	Prenatal diagnosis of chromosome 8p23.1 microdeletion by array comparative genomic hybridization using uncultured amniocytes in a pregnancy associated with fetal partial corpus callosum agenesis and schizencephaly	陳持平(Chih-Ping Chen)*;(Cheng-Ran Peng);(Tung-Yao Chang);(Wan-Yuo Guo);(Yen-Ni Chen);(Peih-Shan Wu);(Dai-Dyi Town);(Wayseen Wang)
中國醫藥大學	2015-10	Prenatal diagnosis and array comparative genomic hybridization characterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13 associated with Langer-Giedion syndrome and Cornelia de Lange syndrome and haploinsufficiency of TRPS1, RAD21 and EXT1	陳持平(Chih-Ping Chen)*;(Ming-Huei Lin);(Yi-Yung Chen);(Schu-Rern Chern);(Yen-Ni Chen);(Peih-Shan Wu);(Chen-Wen Pan);(Meng-Shan Lee);(Wayseen Wang)
中國醫藥大學	2015-08	Mosaic trisomy 15 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review	陳持平(Chih-Ping Chen)*;(Schu-Rern Chern);(Yen-Ni Chen);(Peih-Shan Wu);(Chien-Wen Yang);(Li-Feng Chen);(Wayseen Wang)
中國醫藥大學	2015-06	Distal 3p duplication and terminal 7q deletion associated with nuchal edema and cyclopia in a fetus and a review of the literature	陳持平(Chih-Ping Chen)*;(Ming-Chao Huang);(Schu-Rern Chern);(Yu-Ling Kuo);(Yen-Ni Chen);(Peih-Shan Wu);(Li-Feng Chen);(Chen-Wen Pan);(Wayseen Wang)
中國醫藥大學	2015-04	First-trimester diagnosis of recurrent omphalocele associated with fetal trisomy 18 but without parental mosaicism	陳持平(Chih-Ping Chen)*;(Liang-Kai Wang);(Schu-Rern Chern);(Yu-Ling Kuo);(Yen-Ni Chen);(Chen-Wen Pan);(Wayseen Wang)
中國醫藥大學	2015-02	Detection of no isochromosome 20q by interphase fluorescence in situ hybridization on uncultured amniocytes in a pregnancy with mosaic isochromosome 20q in cultured amniocytes at amniocentesis	陳持平(Chih-Ping Chen)*;蘇俊維(Jun-Wei Su);(Schu-Rern Chern);(Yu-Ling Kuo);(Peih-Shan Wu);(Meng-Shan Lee);(Chien-Wen Yang);(Wayseen Wang)
中國醫藥大學	2015-02	Prenatal diagnosis and array comparative genomic hybridization characterization of trisomy 21 in a fetus associated with right congenital diaphragmatic hernia and a review of the literature of chromosomal abnormalities associated with congenital diap	陳持平(Chih-Ping Chen)*;(Yeou-Lih Wang);(Schu-Rern Chern);(Yu-Peng Liu);(Cheng-Ran Peng);(Yu-Ling Kuo);(Peih-Shan Wu);(Wen-Lin Chen);(Wayseen Wang)
中國醫藥大學	2015-02	Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma	陳持平(Chih-Ping Chen)*;(Tsang-Ming Ko);(Ming-Chao Huang);(Schu-Rern Chern);(Tan-Wei Lin);(Tung-Yao Chang);(Yu-Ling Kuo);(Wen-Lin Chen);(Wayseen Wang)
中國醫藥大學	2014-12	Interphase fluorescence in situ hybridization characterization of mosaicism using uncultured amniocytes and cultured stimulated cord blood lymphocytes in prenatally detected Pallister-Killian syndrome	陳持平(Chih-Ping Chen)*;(Cheng-Ran Peng);(Schu-Rern Chern);(Yu-Ling Kuo);(Peih-Shan Wu);(Dai-Dyi Town);(Chen-Wen Pan);(Chien-Wen Yang);(Wayseen Wang)
中國醫藥大學	2014-12	Prenatal diagnosis and molecular cytogenetic characterization of a 1.07-Mb microdeletion at 5q35.2-q35.3 associated with NSD1 haploinsufficiency and Sotos syndrome	陳持平(Chih-Ping Chen)*;(Chen-Ju Lin);(Schu-Rern Chern);(Yu-Peng Liu);(Yu-Ling Kuo);(Peih-Shan Wu);(Dai-Dyi Town);(Li-Feng Chen);(Chien-Wen Yang);(Wayseen Wang)

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