English  |  正體中文  |  简体中文  |  Items with full text/Total items : 90429/105609 (86%)
Visitors : 10449105      Online Users : 714
RC Version 6.0 © Powered By DSPACE, MIT. Enhanced by NTU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version

    Category

    Loading community tree, please wait....

    Year

    Loading year class tree, please wait....

    Items for Author "Wu), Peih-Shan Wu(Peih-Shan" 

    Return to Browse by Author

    Showing 11 items.

    Collection Date Title Authors Bitstream
    [生物科技學系] 期刊論文 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*; Huang), Ming-Chao Hu(Ming-Chao; Chern), Schu-Rern Ch(Schu-Rern; Kuo), Yu-Ling Kuo(Yu-Ling; Chen), Yen-Ni Chen(Yen-Ni; Wu), Peih-Shan Wu(Peih-Shan; Chen), Li-Feng Chen(Li-Feng; Pan), Chen-Wen Pan(Chen-Wen; Wang), Wayseen Wang(Wayseen
    [生物科技學系] 期刊論文 2015-08 Mosaic trisomy 15 at amniocentesis: prenatal diagnosis, molecular genetic analysis and literature review 陳持平*; Chern), Schu-Rern Ch(Schu-Rern; Chen), Yen-Ni Chen(Yen-Ni; Wu), Peih-Shan Wu(Peih-Shan; Yang), Chien-Wen Ya(Chien-Wen; Chen), Li-Feng Chen(Li-Feng; Wang), Wayseen Wang(Wayseen
    [生物科技學系] 期刊論文 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*; Lin), Ming-Huei Li(Ming-Huei; Chen), Yi-Yung Chen(Yi-Yung; Chern), Schu-Rern Ch(Schu-Rern; Chen), Yen-Ni Chen(Yen-Ni; Wu), Peih-Shan Wu(Peih-Shan; Pan), Chen-Wen Pan(Chen-Wen; Lee), Meng-Shan Le(Meng-Shan; Wang), Wayseen Wang(Wayseen
    [生物科技學系] 期刊論文 2016-02 Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion Chen), Yen-Ni Chen(Yen-Ni; 陳持平*; Ko), Tsang-Ming K(Tsang-Ming; Wang), Liang-Kai Wa(Liang-Kai; Wu), Pei-Chen Wu(Pei-Chen; Chang), Tung-Yao Cha(Tung-Yao; Wu), Peih-Shan Wu(Peih-Shan; Yang), Chien-Wen Ya(Chien-Wen; Wang), Wayseen Wang(Wayseen
    [生物科技學系] 期刊論文 2016-04 Prenatal diagnosis and molecular cytogenetic characterization of a de novo 4.858-Mb microdeletion in 15q14 associated with ACTC1 and MEIS2 haploinsufficiency and tetrology of Fallot Chen)*, 陳持平(Chih-Ping; Chen), Chen-Yu Chen(Chen-Yu; Chern), Schu-Rern Ch(Schu-Rern; Wu), Peih-Shan Wu(Peih-Shan; Chen), Yen-Ni Chen(Yen-Ni; Chen), Shin-Wen Che(Shin-Wen; Chen), Li-Feng Chen(Li-Feng; Yang), Chien-Wen Ya(Chien-Wen; Wang), Wayseen Wang(Wayseen
    [生物科技學系] 期刊論文 2016-04 Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes Chen)*, 陳持平(Chih-Ping; Wang), Yeou-Lih Wan(Yeou-Lih; Chern), Schu-Rern Ch(Schu-Rern; Wu), Peih-Shan Wu(Peih-Shan; Chen), Yen-Ni Chen(Yen-Ni; Chen), Shin-Wen Che(Shin-Wen; Chen), Li-Feng Chen(Li-Feng; Lee), Meng-Shan Le(Meng-Shan; Yang), Chien-Wen Ya(Chien-Wen; Wang), Wayseen Wang(Wayseen
    [生物科技學系] 期刊論文 2016-04 Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3->pter) and partial trisomy 16q (16q23.1->qter) Chen)*, 陳持平(Chih-Ping; Hung), Fang-Yu Hung(Fang-Yu; Chern), Schu-Rern Ch(Schu-Rern; Wu), Peih-Shan Wu(Peih-Shan; Chen), Yen-Ni Chen(Yen-Ni; Chen), Shin-Wen Che(Shin-Wen; Lee), Chen-Chi Lee(Chen-Chi; Wang), Wayseen Wang(Wayseen
    [生物科技學系] 期刊論文 2016-04 Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome Chen)*, 陳持平(Chih-Ping; Ko), Tsang-Ming K(Tsang-Ming; Chern), Schu-Rern Ch(Schu-Rern; Wu), Peih-Shan Wu(Peih-Shan; Chen), Yen-Ni Chen(Yen-Ni; Chen), Shin-Wen Che(Shin-Wen; Chen), Li-Feng Chen(Li-Feng; Yang), Chien-Wen Ya(Chien-Wen; Wang), Wayseen Wang(Wayseen
    [生物科技學系] 期刊論文 2016-06 Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction Chen)*, 陳持平(Chih-Ping; Ko), Tsang-Ming K(Tsang-Ming; Huang), Wen-Chu Huan(Wen-Chu; Chern), Schu-Rern Ch(Schu-Rern; Wu), Peih-Shan Wu(Peih-Shan; Chen), Yen-Ni Chen(Yen-Ni; Chen), Shin-Wen Che(Shin-Wen; Lee), Chen-Chi Lee(Chen-Chi; (Chen-Wen Pan,); Wang), Wayseen Wang(Wayseen
    [生物科技學系] 期刊論文 2016-06 Prenatal diagnosis of mosaic small supernumerary marker chromosome 17 associated with ventricular septal defect, developmental delay and speech delay Chen)*, 陳持平(Chih-Ping; Chiang), Sheng Chiang(Sheng; Wang), Kung-Liahng(Kung-Liahng; Cho), Fu-Nan Cho(Fu-Nan; Chen), Ming Chen(Ming; Chern), Schu-Rern Ch(Schu-Rern; Wu), Peih-Shan Wu(Peih-Shan; Chen), Yen-Ni Chen(Yen-Ni; (Shin-Wen Chen,); (Shun-Ping Chang,); Chen), Weu-Lin Chen(Weu-Lin; Wang), Wayseen Wang(Wayseen
    [生物科技學系] 期刊論文 2016-06 22q13 deletion syndrome in a fetus associated with microtia, hemivertebrae and congenital heart defects on prenatal ultrasound Chen)*, 陳持平(Chih-Ping; Chang), Tung-Yao Cha(Tung-Yao; Wang), Liang-Kai Wa(Liang-Kai; Chern), Schu-Rern Ch(Schu-Rern; Wu), Peih-Shan Wu(Peih-Shan; Chen), Yen-Ni Chen(Yen-Ni; Chen), Shin-Wen Che(Shin-Wen; Chen), Weu-Lin Chen(Weu-Lin; Wang), Wayseen Wang(Wayseen

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library IR team Copyright ©   - Feedback