Search Results - "Tsang-Ming, Ko" :: K.UTB vyhledávací portál

Presymptomatic Diagnosis of Spinal Muscular Atrophy Through Newborn Screening

by Chien, Yin-Hsiu, Chiang, Shu-Chuan, Weng, Wen-Chin, Lee, Ni-Chung, Lin, Ching-Jie, Hsieh, Wu-Shiun, Lee, Wang-Tso, Jong, Yuh-Jyh, Ko, Tsang-Ming, Hwu, Wuh-Liang
Published in The Journal of pediatrics (01.11.2017)

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Incontinentia pigmenti in a male infant and a proposed diagnostic algorithm

by Yang, Min‐Chia, Lin, Yu‐Chen, Huang, Chien‐Hao, Ko, Tsang‐Ming, Tsai, Meng‐Che, Kuo, Pao‐Lin, Lee, Julia Yu‐Yun, McGrath, John A., Hsu, Chao‐Kai
Published in Clinical and experimental dermatology (01.07.2022)

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Massively parallel sequencing analysis of nondegraded and degraded DNA mixtures using the ForenSeq™ system in combination with EuroForMix software

by Hwa, Hsiao-Lin, Wu, Ming-Yih, Chung, Wan-Chia, Ko, Tsang-Ming, Lin, Chih-Peng, Yin, Hsiang-I, Lee, Tsui-Ting, Lee, James Chun-I
Published in International journal of legal medicine (01.01.2019)

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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 and a favorable fetal outcome in a pregnancy

by Chen, Chih-Ping, Ko, Tsang-Ming, Chen, Shin-Wen, Chern, Schu-Rern, Wu, Fang-Tzu, Pan, Yen-Ting, Pan, Chen-Wen, Chen, Yun-Yi, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.05.2023)

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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 Chen, Chih-Ping, Ko, Tsang-Ming, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Shin-Wen, Wu, Fang-Tzu, Chen, Yun-Yi, Lee, Meng-Shan, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.07.2021)

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Prenatal Diagnosis of Placental Mesenchymal Dysplasia with 46, X, Isochromosome Xq/45, X Mosaicism

by Hsu, Chin-Chieh, Lee, Chien-Hong, Chang, Shuenn-Dyh, Ko, Tsang-Ming, Ueng, Shir-Hwa, Chen, Yu-Hsiu, Wang, Mei-Chia, Chang, Yao-Lung
Published in Genes (27.01.2022)

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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 Chen, Chih-Ping, Ko, Tsang-Ming, Chen, Tze-Chien, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Shin-Wen, Wu, Fang-Tzu, Chen, Wen-Lin, Chen, Yun-Yi, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.07.2022)

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Quantifying the legacy of the Chinese Neolithic on the maternal genetic heritage of Taiwan and Island Southeast Asia

by Brandão, Andreia, Eng, Ken Khong, Rito, Teresa, Cavadas, Bruno, Bulbeck, David, Gandini, Francesca, Pala, Maria, Mormina, Maru, Hudson, Bob, White, Joyce, Ko, Tsang-Ming, Saidin, Mokhtar, Zafarina, Zainuddin, Oppenheimer, Stephen, Richards, Martin B., Pereira, Luísa, Soares, Pedro
Published in Human genetics (01.04.2016)

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Prenatal diagnosis of maternal uniparental disomy 16 associated with mosaic trisomy 16 at amniocentesis, and pericardial effusion and intrauterine growth restriction in the fetus

by Chen, Chih-Ping, Ko, Tsang-Ming, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Shin-Wen, Wu, Fang-Tzu, Chen, Yun-Yi, Town, Dai-Dyi, Chen, Li-Feng, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.05.2021)

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Prenatal diagnosis of low-level mosaicism for trisomy 21 by amniocentesis in a pregnancy associated with maternal uniparental disomy of chromosome 21 in the fetus and a favorable outcome

by Chen, Chih-Ping, Ko, Tsang-Ming, Chen, Yi-Yung, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Shin-Wen, Wu, Fang-Tzu, Chen, Yun-Yi, Chen, Wen-Lin, Pan, Chen-Wen, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.09.2020)

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Prenatal diagnosis of low-level mosaicism for a small supernumerary marker chromosome derived from chromosome 9q (9q13-q21.33) in a pregnancy with a favorable outcome, and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes

by Chen, Chih-Ping, Lo, Liang-Ming, Ko, Tsang-Ming, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Shin-Wen, Wu, Fang-Tzu, Town, Dai-Dyi, Chen, Li-Feng, Chen, Yun-Yi, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.03.2021)

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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 a pregnancy associated with increased nuchal translucency and an abnormal maternal serum screening result

by Chen, Chih-Ping, Ko, Tsang-Ming, Wang, Liang-Kai, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Shin-Wen, Wu, Fang-Tzu, Chen, Li-Feng, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.07.2021)

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Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 15 at amniocentesis

by Chen, Chih-Ping, Hsu, Te-Yao, Ko, Tsang-Ming, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Shin-Wen, Wu, Fang-Tzu, Chen, Yun-Yi, Lee, Chen-Chi, Pan, Chen-Wen, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.09.2020)

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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 in DYNC2H1 in a fetus

by Chen, Chih-Ping, Ko, Tsang-Ming, Chang, Tung-Yao, Chern, Schu-Rern, Chen, Shin-Wen, Lai, Shih-Ting, Chuang, Tzu-Yun, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.02.2018)

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Prenatal diagnosis of a familial normal euchromatic variant of dup(15)(q11.2q11.2) in a pregnancy with a favorable outcome

by Chen, Chih-Ping, Ko, Tsang-Ming, Huang, Jian-Pei, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Shin-Wen, Wu, Fang-Tzu, Chen, Wen-Lin, Lee, Meng-Shan, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.09.2020)

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Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 1q42.3-q44 deletion in a fetus associated with ventriculomegaly on prenatal ultrasound

by Chen, Chih-Ping, Ko, Tsang-Ming, Wang, Liang-Kai, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Shin-Wen, Wu, Fang-Tzu, Chen, Yun-Yi, Chen, Wen-Lin, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.07.2020)

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

by Chen, Chih-Ping, Ko, Tsang-Ming, Wang, Liang-Kai, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Shin-Wen, Wu, Fang-Tzu, Chen, Li -Feng, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.09.2019)

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

by Chen, Chih-Ping, Ko, Tsang-Ming, Chen, Chen-Yu, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Shin-Wen, Wu, Fang-Tzu, Pan, Chen-Wen, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.11.2019)

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Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome

by Chen, Chih-Ping, Ko, Tsang-Ming, Chen, Yi-Yung, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Shin-Wen, Lai, Shih-Ting, Chuang, Tzu-Yun, Yang, Chien-Wen, Pan, Chen-Wen, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.12.2017)

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Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities

by Chen, Chih-Ping, Ko, Tsang-Ming, Wang, Liang-Kai, Chern, Schu-Rern, Wu, Peih-Shan, Chen, Shin-Wen, Lai, Shih-Ting, Chuang, Tzu-Yun, Yang, Chien-Wen, Lee, Chen-Chi, Wang, Wayseen
Published in Taiwanese journal of obstetrics & gynecology (01.02.2018)

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