Search Results - "cytogenetics"

Prenatal diagnosis and molecular cytogenetic characterization of a chromosome 1q42.3-q44 deletion in a fetus associated with ventriculomegaly on prenatal ultrasound by Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Wen-Lin Chen, Wayseen Wang

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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

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Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 15 in a pregnancy associated with recurrent Down syndrome by Chih-Ping Chen, Chia-Hao Chan, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Dai-Dyi Town, Meng-Shan Lee, Wayseen Wang

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Prenatal diagnosis and molecular cytogenetic characterization of an interstitial deletion of 18q12.1-q12.3 encompassing DTNA, CELF4 and SETBP1 by Chih-Ping Chen, Chih-Heng Hsieh, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Chen-Chi Lee, Wayseen Wang

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Anomalies in Human Sex Determination: Usefulness of a Combined Cytogenetic Approach to Characterize an Additional Case with Xp Functional Disomy Associated with 46,XY Gonadal Dysgenesis by Rjiba Khouloud, Wafa Slimani, Meriem Gaddas, Ikbel Hadj hassine, Afef Jelloul, Hela Ben Khelifa, Fethi El Amri, Monia Zaouali, Kenneth Mcelreavey, Ali Saad, Soumaya Mougou-Zerelli

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Prenatal diagnosis and molecular cytogenetic characterization of a mosaic derivative Y chromosome derived from a de novo unbalanced reciprocal Yq;13q translocation by Chih-Ping Chen, Yi-Ning Su, Ming Chen, Jain-Pei Huang, Fuu-Jen Tsai, Pei-Chen Wu, Wen-Lin Chen, Wayseen Wang

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Prenatal diagnosis of mosaic trisomy 18 and maternal uniparental disomy 18 by amniocentesis in a pregnancy associated with cytogenetic discrepancy in various tissues and a favorable fetal outcome by Chih-Ping Chen, Fang-Tzu Wu, Yen-Ting Pan, Schu-Rern Chern, Peih-Shan Wu, Chien-Ling Chiu, Chen-Chi Lee, Wen-Lin Chen, Wayseen Wang

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Cytogenetic discrepancy between uncultured amniocytes and cultured amniocytes in mosaic trisomy 18 at amniocentesis in a pregnancy with a favorable fetal outcome and maternal uniparental disomy 18 by Chih-Ping Chen, Jun-Wei Su, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wen-Lin Chen, Meng-Shan Lee, Chen-Wen Pan, Yun-Yi Chen, Wayseen Wang

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A de novo duplication of chromosome 21q22.11→qter associated with Down syndrome: Prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings by Chih-Ping Chen, Hsu-Kuang Huang, Pei-Ying Ling, Yi-Ning Su, Ming Chen, Fuu-Jen Tsai, Pei-Chen Wu, Schu-Rern Chern, Yu-Ting Chen, Chen-Chi Lee, Wayseen Wang

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Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome by Chih-Ping Chen, Tsang-Ming Ko, Liang-Kai Wang, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chien-Wen Yang, Dai-Dyi Town, Meng-Shan Lee, Wayseen Wang

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Low-level mosaic trisomy 6 at amniocentesis can be a culture artefact and associated with a favorable outcome and cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes by Chih-Ping Chen

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Wheat Evolution and Domestication by Feldman, Moshe

Subjects: “…cytogenetics…”
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Genetics, Evolution, and Conservation of Neotropical Fishes

Subjects: “…Fish cytogenetics…”
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Wheat Evolution and Domestication by Feldman, Moshe

Subjects: “…cytogenetics…”
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OAPEN Library: description of the publication

Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 7 in the male partner of a phenotypically normal couple with repeated spontaneous abortions by Chih-Ping Chen, Ming Chen, Yuh-Ming Hwu, Shun-Ping Chang, Shin-Wen Chen, Shih-Ting Lai, Chen-Chi Lee, Wayseen Wang

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Prenatal diagnosis and molecular cytogenetic characterization of partial dup(18q)/del(18p) due to a paternal pericentric inversion 18 in a fetus with multiple anomalies by Min Jin Lee, Sang Hee Park, Sung Han Shim, Myoung-jin Moon, Dong Hyun Cha

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Características clínicas e citogenéticas da síndrome de Turner na região Centro-Oeste do Brasil Clinical and cytogenetic aspects of the Turner syndrome in the Brazilian Western region by Claudinéia de Araújo, Bianca Borsatto Galera, Marcial Francis Galera, Sebastião Freitas de Medeiros

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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

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Mosaic tetrasomy 9p at amniocentesis in a pregnancy associated with a favorable fetal outcome, perinatal progressive decrease of the aneuploid cell line and cytogenetic discrepancy in various tissues by Chih-Ping Chen, Shin-Wen Chen, Schu-Rern Chern, Peih-Shan Wu, Fang-Tzu Wu, Yen-Ting Pan, Chen-Chi Lee, Chen-Wen Pan, Yun-Yi Chen, Wayseen Wang

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Prenatal diagnosis of mosaic trisomy 2: Discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction by Chih-Ping Chen, Yi-Ning Su, Shin-Yu Lin, Schu-Rern Chern, Yu-Ting Chen, Meng-Shan Lee, Wayseen Wang

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