Hasil Pencarian - Tsang-Ming Ko

Perbaiki Hasil
  1. 1
    Prenatal Diagnosis and Genetic Analysis of a Fetus with 47,XX, +21/46,XX Mosaicism and XX/XY Chimerism

    Prenatal Diagnosis and Genetic Analysis of a Fetus with 47,XX, +21/46,XX Mosaicism and XX/XY Chimerism oleh Hsiao-Lin Hwa, Tsang-Ming Ko, Chien-Hao Huang, Li-Shu Chang

    Diterbitkan 2006-01-01
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  2. 2
    First-trimester molecular diagnosis of complete hydatidiform mole associated with dizygotic twin pregnancy conceived by intrauterine insemination

    First-trimester molecular diagnosis of complete hydatidiform mole associated with dizygotic twin pregnancy conceived by intrauterine insemination oleh Chih-Ping Chen, Tsang-Ming Ko, Chen-Yu Chen, Tao-Yeuan Wang, Schu-Rern Chern, Yu-Ling Kuo, Wayseen Wang

    Diterbitkan 2014-12-01
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  3. 3
    Mosaic trisomy 14 at amniocentesis: Prenatal diagnosis and literature review

    Mosaic trisomy 14 at amniocentesis: Prenatal diagnosis and literature review oleh Chih-Ping Chen, Kuo-Gon Wang, Tsang-Ming Ko, Schu-Rern Chern, Jun-Wei Su, Dai-Dyi Town, Wayseen Wang

    Diterbitkan 2013-09-01
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  4. 4
    Multiplex Ligation-dependent Probe Amplification Identification of Deletions and Duplications of the Duchenne Muscular Dystrophy Gene in Taiwanese Subjects

    Multiplex Ligation-dependent Probe Amplification Identification of Deletions and Duplications of the Duchenne Muscular Dystrophy Gene in Taiwanese Subjects oleh Hsiao-Lin Hwa, Yih-Yuan Chang, Chung-Hsiung Chen, Yen-Shi Kao, Yuh-Jyh Jong, Mei-Chyn Chao, Tsang-Ming Ko

    Diterbitkan 2007-05-01
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  5. 5
    Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations in DYNC2H1 in a fetus

    Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly (SRTD3) associated with compound heterozygous mutations... oleh Chih-Ping Chen, Tsang-Ming Ko, Tung-Yao Chang, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Wayseen Wang

    Diterbitkan 2018-02-01
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  6. 6
    Prenatal diagnosis of mosaic tetrasomy 18p

    Prenatal diagnosis of mosaic tetrasomy 18p oleh Chih-Ping Chen, Tsang-Ming Ko, Yi-Ning Su, Schu-Rern Chern, Jun-Wei Su, Yu-Ting Chen, Dai-Dyi Town, Wayseen Wang

    Diterbitkan 2012-12-01
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  7. 7
    Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2→q11.21)

    Prenatal diagnosis and molecular cytogenetic characterization of a proximal deletion of 22q (22q11.2→q11.21) oleh Chih-Ping Chen, Tsang-Ming Ko, Yi-Ning Su, Jun-Wei Su, Yu-Ting Chen, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang

    Diterbitkan 2013-03-01
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  8. 8
    Small Mutations of the DMD Gene in Taiwanese Families

    Small Mutations of the DMD Gene in Taiwanese Families oleh Hsiao-Lin Hwa, Yih-Yuan Chang, Chien-Hao Huang, Chung-Hsiung Chen, Yen-Shi Kao, Yuh-Jyh Jong, Mei-Chyn Chao, Tsang-Ming Ko

    Diterbitkan 2008-06-01
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  9. 9
    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16

    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16 oleh Chih-Ping Chen, Tsang-Ming Ko, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Chien-Wen Yang, Chen-Wen Pan, Wayseen Wang

    Diterbitkan 2017-08-01
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  10. 10
    Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result

    Prenatal diagnosis of partial monosomy 8p (8p23.2→pter) and partial trisomy 15q (15q21.2→qter) and incidental detection of a familial chromosome translocation of paternal origin in... oleh Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Li-Feng Chen, Wayseen Wang

    Diterbitkan 2021-07-01
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  11. 11
    Low-level mosaic trisomy 9 at amniocentesis associated with a positive non-invasive prenatal testing for trisomy 9, maternal uniparental disomy 9, intrauterine growth restriction and a favorable fetal outcome in a pregnancy

    Low-level mosaic trisomy 9 at amniocentesis associated with a positive non-invasive prenatal testing for trisomy 9, maternal uniparental disomy 9, intrauterine growth restriction a... oleh Chih-Ping Chen, Tsang-Ming Ko, Shin-Wen Chen, Schu-Rern Chern, Fang-Tzu Wu, Yen-Ting Pan, Chen-Wen Pan, Yun-Yi Chen, Wayseen Wang

    Diterbitkan 2023-05-01
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  12. 12
    Prenatal diagnosis of partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31→qter) associated with increased nuchal translucency and abnormal maternal serum biochemistry in the first trimester

    Prenatal diagnosis of partial trisomy 16p (16p12.2→pter) and partial monosomy 22q (22q13.31→qter) associated with increased nuchal translucency and abnormal maternal serum biochemi... oleh Chih-Ping Chen, Tsang-Ming Ko, Yi-Ning Su, Chin-Yuan Hsu, Yi-Yung Chen, Jun-Wei Su, Wen-Lin Chen, Chen-Wen Pan, Wayseen Wang

    Diterbitkan 2012-03-01
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  13. 13
    Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma

    Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma oleh Chih-Ping Chen, Tsang-Ming Ko, Ming-Chao Huang, Schu-Rern Chern, Tan-Wei Lin, Tung-Yao Chang, Yu-Ling Kuo, Wen-Lin Chen, Wayseen Wang

    Diterbitkan 2015-02-01
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  14. 14
    Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion

    Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion oleh Yen-Ni Chen, Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Pei-Chen Wu, Tung-Yao Chang, Peih-Shan Wu, Chien-Wen Yang, Wayseen Wang

    Diterbitkan 2016-02-01
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  15. 15
    Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization

    Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization oleh Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Li -Feng Chen, Wayseen Wang

    Diterbitkan 2019-09-01
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  16. 16
    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3

    Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3 oleh Chih-Ping Chen, Tsang-Ming Ko, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Chen-Wen Pan, Wayseen Wang

    Diterbitkan 2019-11-01
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  17. 17
    Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome

    Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome oleh Chih-Ping Chen, Tsang-Ming Ko, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Li-Feng Chen, Chien-Wen Yang, Wayseen Wang

    Diterbitkan 2016-04-01
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  18. 18
    Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid confirmation of low-level mosaicism for tetrasomy 18p

    Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid confirmation of low-level mosaicism for tetrasomy 18p oleh Chih-Ping Chen, Chen-Li Lin, Tsang-Ming Ko, Schu-Rern Chern, Yu-Ting Chen, Peih-Shan Wu, Yu-Ling Kuo, Meng-Shan Lee, Wayseen Wang

    Diterbitkan 2014-03-01
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  19. 19
    Mosaic Xq duplication, or 46,X,der(X)dup(X)(q22.1q22.2)dup(X)(q25q22.3)/ 46,XX at amniocentesis in a pregnancy with a favorable outcome

    Mosaic Xq duplication, or 46,X,der(X)dup(X)(q22.1q22.2)dup(X)(q25q22.3)/ 46,XX at amniocentesis in a pregnancy with a favorable outcome oleh Chih-Ping Chen, Tsang-Ming Ko, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Meng-Shan Lee, Wayseen Wang

    Diterbitkan 2021-07-01
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  20. 20
    Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 21

    Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 21 oleh Chih-Ping Chen, Chyi-Chyang Lin, Tsang-Ming Ko, Fuu-Jen Tsai, Schu-Rern Chern, Chen-Chi Lee, Yu-Ting Chen, Pei-Chen Wu, Wayseen Wang

    Diterbitkan 2010-09-01
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