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    Items for Author "Schu-Rern Ch" 

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    Showing 16 items.

    Collection Date Title Authors Bitstream
    [生物科技學系] 期刊論文 2017-08 Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect 陳持平; Chih-Ping Chen; Chen-Yu Chen; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Chen-Chi Lee; Chien-Wen Ya; Chien-Wen Yang; Wayseen Wang
    [生物科技學系] 期刊論文 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
    [生物科技學系] 期刊論文 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
    [生物科技學系] 期刊論文 2017-08 Prenatal diagnosis of mosaicism for trisomy 2 in a single colony at amniocentesis in a pregnancy with a favorable outcome 陳持平; Chih-Ping Chen; Jian-Pei Hua; Jian-Pei Huang; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Chen-Chi Lee; Chien-Wen Ya; Chien-Wen Yang; Wayseen Wang
    [生物科技學系] 期刊論文 2017-08 Detection of paternal uniparental disomy 9 in a neonate with prenatally detected mosaicism for a small supernumerary marker chromosome 9 and a supernumerary ring chromosome 9 陳持平; Chih-Ping Chen; Ming Chen; Liang-Kai Wa; Liang-Kai Wang; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Shun-Ping Ch; Shun-Ping Chang; Chien-Wen Ya; Chien-Wen Yang; Chen-Wen Pan; Wayseen Wang
    [生物科技學系] 期刊論文 2017-06 Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 20p ；20p12-p13 encompassing JAG1 and a literature review of prenatal diagnosis of Alagille syndrome 陳持平; Chih-Ping Chen; Chang-Sheng; Chang-Sheng Yin; Liang-Kai Wa; Liang-Kai Wang; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Wen-Lin Chen; Wayseen Wang
    [生物科技學系] 期刊論文 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
    [生物科技學系] 期刊論文 2017-06 Molecular genetic characterization of a prenatally detected de novo interstitial deletion of chromosome 2q ；2q31.1-q32.1 encompassing HOXD13, ZNF385B and ZNF804A associated with syndactyly and increased first-trimester nuchal translucency 陳持平; Chih-Ping Chen; Chen-Ju Lin; Yen-Ni Chen; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Li-Feng Chen; Wayseen Wang
    [生物科技學系] 期刊論文 2017-06 Pfeiffer syndrome with FGFR2 C342R mutation presenting extreme proptosis, craniosynostosis, hearing loss, ventriculomegaly, broad great toes and thumbs, maxillary hypoplasia, and laryngomalacia 陳持平; Chih-Ping Chen; Shuan-Pei Li; Shuan-Pei Lin; Yu-Peng Liu; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Wayseen Wang
    [生物科技學系] 期刊論文 2017-06 Molecular genetic characterization of a prenatally detected 1.484-Mb Xq13.3-q21.1 duplication encompassing ATRX and a literature review of syndromic intellectual disability and congenital abnormalities in males with a duplication at Xq13.3-q21.1 陳持平; Chih-Ping Chen; Hoi-Kin Yip; Liang-Kai Wa; Liang-Kai Wang; Schu-Rern Ch; Schu-Rern Chern; Shin-Wen Che; Shin-Wen Chen; Shih-Ting La; Shih-Ting Lai; Peih-Shan Wu; Wayseen Wang
    [生物科技學系] 期刊論文 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
    [生物科技學系] 期刊論文 2017-04 Detection of mosaic 15q11.1-q11.2 deletion encompassing NBEAP1 and POTEB in a fetus with diffuse lymphangiomatosis 陳持平; Chih-Ping Chen; Kuo-Gon Wang; Hsu-Kuang Hu; Hsu-Kuang Huang; Cheng-Ran Pe; Cheng-Ran Peng; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Che; Shin-Wen Chen; Chen-Chi Lee; Wayseen Wang
    [生物科技學系] 期刊論文 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
    [生物科技學系] 期刊論文 2017-04 Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome 陳持平; Chih-Ping Chen; Tsang-Ming K; Tsang-Ming Ko; Liang-Kai Wa; Liang-Kai Wang; Shuan-Pei Li; Shuan-Pei Lin; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Che; Shin-Wen Chen; Meng-Shan Le; Meng-Shan Lee; Wayseen Wang
    [生物科技學系] 期刊論文 2017-04 Prenatal diagnosis of mosaicism for trisomy 15 in a single colony at amniocentesis with a favorable fetal outcome 陳持平; Chih-Ping Chen; Fang-Yu Hung; Schu-Rern Ch; Schu-Rern Chern; Peih-Shan Wu; Yen-Ni Chen; Shin-Wen Che; Shin-Wen Chen; Chien-Wen Ya; Chien-Wen Yang; Wen-Lin Chen; Wayseen Wang
    [生物科技學系] 期刊論文 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

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