English  |  正體中文  |  简体中文  |  Items with full text/Total items : 90074/105197 (86%)
Visitors : 7165706      Online Users : 43
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 "Wang), Wayseen Wang(Wayseen" 

    Return to Browse by Author

    Showing 12 items.

    Collection Date Title Authors Bitstream
    [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
    [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 2016-02 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 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 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 2015-08 Pregnancy with de novo 9q34.3 microdeletion and Kleefstra syndrome in the fetus may be associated with an abnormal maternal serum screening result 陳持平*; Lin), Shuan-Pei Li(Shuan-Pei; Li), Hui-Bo Li(Hui-Bo; Chen), Yen-Ni Chen(Yen-Ni; Wang), Wayseen Wang(Wayseen
    [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

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