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    显示项目2376-2400 / 3308. (共133页)
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    日期题名作者
    2017-04 Prenatal diagnosis and molecular cytogenetic characterization of concomitant familial small supernumerary marker chromosome derived from chromosome 4q ；4q11.1-q13.2 and 5q13.2 microdeletion with no apparent phenotypic abnormality 陳持平; Chih-Ping Chen; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Che; Shin-Wen Chen; Chien-Wen Ya; Chien-Wen Yang; Chen-Chi Lee; Meng-Shan Le; Meng-Shan Lee
    2016-04 Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3->pter) and partial trisomy 16q (16q23.1->qter) Wang；, 陳持平；Chih-Ping Chen；*；Fang-Yu Hung；Fang-Yu Hung；Schu-Rern Ch；Schu-Rern Chern；Peih-Shan Wu；Peih-Shan Wu；Yen-Ni Chen；Yen-Ni Chen；Shin-Wen Che；Shin-Wen Chen；Chen-Chi Lee；Chen-Chi Lee；Wayseen Wang；Wayseen
    2016-04 Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p (3p26.3->pter) and partial trisomy 16q (16q23.1->qter) 陳持平; Chen, Chih-Ping; *; Hung, Fang-Yu; Hung, Fang-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen
    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
    2016-04 Prenatal diagnosis and molecular cytogenetic characterization of de novo partial monosomy 3p ;3p26.3->pter; and partial trisomy 16q ;16q23.1->qter; 陳持平; Chen, Chih-Ping; *; Hung, Fang-Yu; Hung, Fang-Yu; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Lee, Chen-Chi; Lee, Chen-Chi; Wang, Wayseen; Wang, Wayseen
    2013-03 Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 12q (12q24.21->qter) and partial monosomy 6q (6q27->qter) associated with coarctation of the aorta, ventriculomegaly and thickened nuchal fold 陳持平; Chen, Chih-Ping; Yi-Yung Chen; Schu-Rern Chern; Peih-Shan Wu; Jun-Wei Su; Yu-Ting Chen; Li-Feng Chen; Wayseen Wang
    2010-09 Prenatal diagnosis and molecular cytogenetic characterization of de novo partial trisomy 7p (7p15.3->pter) and partial monosomy 13q (13q33.3->qter) associated with Dandy-Walker malformation, abnormal skull development and microcephaly 陳持平; Chen, Chih-Ping; Chen, Ming; Su, Yi-Ning; Tsai, Fuu-Jen; Chern, Schu-Rern; Hsu, Chin-Yuan; Wu, Pei-Chen; Town, Dai-Dyi; Lee, Dong-Jay; Ma, Gwo-Chin; Wang, Wayseen
    2014-02 Prenatal diagnosis and molecular cytogenetic characterization of de novo pure partial trisomy 6p associated with microcephaly, craniosynostosis and abnormal maternal serum biochemistry 陳持平; Chen, Chih-Ping; Ming Cheng; Chen-Yu Chen; Schu-Rern Chern; Peih-Shan Wu; Shun-Ping Chang; Yu-Ling Kuo; Wen-Lin Chen; Chen-Wen Pan; Wayseen Wang
    2017-04 Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome 陳持平; Chih-Ping Chen; Chen-Ju Lin; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Che; Shin-Wen Chen; Chen-Wen Pan; Chien-Wen Ya; Chien-Wen Yang; Wayseen Wang
    2017-12 Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome 陳持平; Chen, Chih-Ping; Tsang-Ming, K; Ko, Tsang-Ming; Chen, Yi-Yung; Ch, Schu-Rern; Chern, Schu-Rern; Che, Shin-Wen; Chen, Shin-Wen; La, Shih-Ting; Lai, Shih-Ting; Chua, Tzu-Yun; Chuang, Tzu-Yun; Ya, Chien-Wen; Yang, Chien-Wen; Pan, Chen-Wen; Wang, Wayseen
    2016-04 Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes 陳持平; Chen, Chih-Ping; *; Wan, Yeou-Lih; Wang, Yeou-Lih; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Chen, Shin-Wen; Chen, Li-Feng; Chen, Li-Feng; Le, Meng-Shan; Lee, Meng-Shan; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen
    2016-04 Prenatal diagnosis and molecular cytogenetic characterization of low-level true mosaicism for trisomy 21 using uncultured amniocytes Wang；, 陳持平；Chih-Ping Chen；*；Yeou-Lih Wan；Yeou-Lih Wang；Schu-Rern Ch；Schu-Rern Chern；Peih-Shan Wu；Peih-Shan Wu；Yen-Ni Chen；Yen-Ni Chen；Shin-Wen Che；Shin-Wen Chen；Li-Feng Chen；Li-Feng Chen；Meng-Shan Le；Meng-Shan Lee；Chien-Wen Ya；Chien-Wen Yang；Wayseen Wang；Wayseen
    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
    2013-10 Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13 陳持平; Chen, Chih-Ping; Chin-Han Tsai; Schu-Rern Chern; Peih-Shan Wu; Jun-Wei Su; Chen-Chi Lee; Yu-Ting Chen; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang
    2013-10 Prenatal diagnosis and molecular cytogenetic characterization of mosaic ring chromosome 13 陳持平; Chen, Chih-Ping; Chin-Han Tsai; Schu-Rern Chern; Peih-Shan Wu; Jun-Wei Su; Chen-Chi Lee; Yu-Ting Chen; Wen-Lin Chen; Li-Feng Chen; Wayseen Wang
    2017-06 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 11 陳持平; Chih-Ping Chen; Ming Chen; Pu-Tsui Wang; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Shun-Ping Ch; Shun-Ping Chang; Chen-Wen Pan; Wayseen Wang
    2014-03 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 15 陳持平; Chen, Chih-Ping; Chen, Ming; Chen, Ming; Su, Yi-Ning; Chern, Schu-Rern; Wu, Peih-Shan; Ch, Shun-Ping; Kuo, Yu-Ling; Chen, Wen-Lin; Wang, Wayseen
    2017-08 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16 陳持平; Chih-Ping Chen; Tsang-Ming K; Tsang-Ming Ko; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Chien-Wen Ya; Chien-Wen Yang; Chen-Wen Pan; Wayseen Wang
    2017-04 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 2 陳持平; Chih-Ping Chen; Ming Chen; Shun-Ping Ch; Shun-Ping Chang; Fang-Yu Hung; Meng-Ju Lee; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Chen; Chen-Chi Lee; Dai-Dyi Town; Meng-Shan Le; Meng-Shan Lee; Wen-Lin Chen; Wayseen Wang
    2017-08 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 21q11.2-q21.1 and a literature review 陳持平; Chih-Ping Chen; Ming Chen; Chia-Hsun Wu; Chen-Ju Lin; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Che; Shin-Wen Chen; Shun-Ping Ch; Shun-Ping Chang; Li-Feng Chen; Wayseen Wang
    2013-09 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome 陳持平; Chen, Chih-Ping; Tsang-Ming, K; Ko, Tsang-Ming; Chen, Yi-Yung; Su, Jun-Wei; Wang, Wayseen
    2012-09 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2 陳持平; Chen, Chih-Ping; Jun-Wei Su,; Alan Hwa-Ruey Hsieh,; Hsieh, Alex Hwa-Jiun; Wang, Wayseen
    2011-06 Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4 陳持平; Chen, Chih-Ping
    2016-10 Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentirc inversion 陳持平; Chen, Chih-Ping; *; Tsang-Ming, K; Ko, Tsang-Ming; Su, Yi-Ning; Su, Yi-Ning; Wa, Liang-Kai; Wang, Liang-Kai; Ch, Schu-Rern; Chern, Schu-Rern; Wu, Peih-Shan; Wu, Peih-Shan; Chen, Yen-Ni; Chen, Yen-Ni; Che, Shin-Wen; Che, Shin-Wen; Town, Dai-Dyi; Town, Dai-Dyi; Chen, Li-Feng; Chen, Li-Feng; Ya, Chien-Wen; Yang, Chien-Wen; Wang, Wayseen; Wang, Wayseen
    2012-06 Prenatal diagnosis and molecular genetic analysis of short rib-polydactyly syndrome type III (Verma-Naumoff) in a second-trimester fetus with a homozygous splice site mutation in intron 4 in the NEK1 gene 陳持平; Chen, Chih-Ping

    显示项目2376-2400 / 3308. (共133页)
    << < 91 92 93 94 95 96 97 98 99 100 > >>
    每页显示[10|25|50]项目

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