Search Results - Tsang-Ming Ko

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

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

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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... by Chih-Ping Chen, Tsang-Ming Ko, Tung-Yao Chang, Schu-Rern Chern, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Wayseen Wang

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

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

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Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 16 by 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

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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... by 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

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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... by 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

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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... by 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

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Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma by 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

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Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion by 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

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Inv dup del(10p): Prenatal diagnosis and molecular cytogenetic characterization by 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

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Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3 by 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

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Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome by 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

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Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid confirmation of low-level mosaicism for tetrasomy 18p by 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

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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 by 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

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Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 21 by 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

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Prenatal diagnosis and molecular cytogenetic characterization of chromosome 22q11.2 deletion syndrome associated with congenital heart defects by Yu-Ling Kuo, Chih-Ping Chen, Liang-Kai Wang, Tsang-Ming Ko, Tung-Yao Chang, Schu-Rern Chern, Peih-Shan Wu, Yu-Ting Chen, Shu-Yuan Chang

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Prenatal Diagnosis and Molecular Cytogenetic Characterization of a Small Supernumerary Marker Chromosome Derived From Chromosome 8 by Chih-Ping Chen, Ming Chen, Tsang-Ming Ko, Gwo-Chin Ma, Fuu-Jen Tsai, Ming-Song Tsai, Pei-Chen Wu, Chen-Chi Lee, Li-Feng Chen, Wayseen Wang

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Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis in a pregnancy with a favorable outcome by Chih-Ping Chen, Tsang-Ming Ko, Tze-Chien Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wen-Lin Chen, Yun-Yi Chen, Wayseen Wang

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