Showing 1 - 10 results of 10 for search 'Yi-Hui Lin', query time: 0.09s Refine Results
  1. 1
    Third-trimester Spontaneous Rupture of an Unscarred Uterus with Massive Intra-abdominal Hemorrhage During Tocolysis in a Pregnant Woman who has had Multiple Instrumental Abortions

    Third-trimester Spontaneous Rupture of an Unscarred Uterus with Massive Intra-abdominal Hemorrhage During Tocolysis in a Pregnant Woman who has had Multiple Instrumental Abortions by Yi-Hui Lin, Chih-Ping Chen, Jen-Ru Lin, Li-Fan Yeh, Tze-Chien Chen

    Published 2004
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  2. 2
    Malignant Fibrous Histiocytoma During Pregnancy: a Case Report

    Malignant Fibrous Histiocytoma During Pregnancy: a Case Report by Hung-Wen Su, Chun-Sen Hsu, Yi-Hui Lin, Ming-I Hsu, Huihua Kenny Chiang, Szu-Yuan Chou

    Published 2006
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  3. 3
    Prenatal diagnosis of a de novo interstitial deletion of chromosome 20q12 in a fetus with complex congenital heart defects, corpus callosum agenesis and intrauterine growth restriction

    Prenatal diagnosis of a de novo interstitial deletion of chromosome 20q12 in a fetus with complex congenital heart defects, corpus callosum agenesis and intrauterine growth restric... by Yi-Hui Lin, Chih-Ping Chen, Tze-Chien Chen, Chun-Sen Hsu, Szu-Yuan Chou, Shu-Chin Chien

    Published 2011
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  4. 4
    Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality

    Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality by Chih-Ping Chen, Chung-Hu Fu, Yi-Hui Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Wayseen Wang

    Published 2016
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  5. 5
    Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic double trisomy involving trisomy 7 and trisomy 20 (48,XY,+7,+20) at amniocentesis

    Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic double trisomy involving trisomy 7 and trisomy 20 (48,XY,+7,+20) at amniocentesis by Chih-Ping Chen, Yi-Hui Lin, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Meng-Shan Lee, Yun-Yi Chen, Wayseen Wang

    Published 2020
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  6. 6
    Mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: Prenatal diagnosis, molecular cytogenetic characterization, and association with 2-Mb deletion of 21q21.1-q21.2 and 5-Mb deletion of 21q22.3

    Mosaic ring chromosome 21, monosomy 21, and isodicentric ring chromosome 21: Prenatal diagnosis, molecular cytogenetic characterization, and association with 2-Mb deletion of 21q21... by Chih-Ping Chen, Yi-Hui Lin, Szu-Yuan Chou, Yi-Ning Su, Schu-Rern Chern, Yu-Ting Chen, Dai-Dyi Town, Wen-Lin Chen, Wayseen Wang

    Published 2012
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  7. 7
    Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormalities

    Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12→q13.1::) associated with phenotypic abnormal... by Chih-Ping Chen, Shuan-Pei Lin, Yi-Hui Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chien-Wen Yang, Wen-Lin Chen, Wayseen Wang

    Published 2016
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  8. 8
    Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic trisomy 20 at amniocentesis in a pregnancy with a favorable outcome

    Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic trisomy 20 at amniocentesis in a pregnancy with a favorable outcome by Chih-Ping Chen, Yi-Hui Lin, Peih-Shan Wu, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Chen-Chi Lee, Chen-Wen Pan, Yun-Yi Chen, Wayseen Wang

    Published 2022
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  9. 9
    Mosaic Ring Chromosome 18, Ring Chromosome 18 Duplication/Deletion and Disomy 18: Perinatal Findings and Molecular Cytogenetic Characterization by Fluorescence In Situ Hybridization and Array Comparative Genomic Hybridization

    Mosaic Ring Chromosome 18, Ring Chromosome 18 Duplication/Deletion and Disomy 18: Perinatal Findings and Molecular Cytogenetic Characterization by Fluorescence In Situ Hybridizatio... by Chih-Ping Chen, Yung-Ting Kuo, Shuan-Pei Lin, Yi-Ning Su, Yann-Jang Chen, Rui-Yuan Hsueh, Yi-Hui Lin, Pei-Chen Wu, Chen-Chi Lee, Yu-Ting Chen, Wayseen Wang

    Published 2010
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  10. 10
    Chromosome 15q overgrowth syndrome: Prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3)

    Chromosome 15q overgrowth syndrome: Prenatal diagnosis, molecular cytogenetic characterization, and perinatal findings in a fetus with dup(15)(q26.2q26.3) by Chih-Ping Chen, Yi-Hui Lin, Heng-Kien Au, Yi-Ning Su, Chin-Yuan Hsu, Yu-Peng Liu, Pei-Chen Wu, Schu-Rern Chern, Yu-Ting Chen, Li-Feng Chen, Adam Hwa-Ming Hsieh, Wayseen Wang

    Published 2011
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