Search Results - "Molecular Cytogenetics"

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  1. 41
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    Prenatal findings and molecular cytogenetic analyses of a de novo interstitial deletion of 1q23.3 encompassing PBX1 gene by Manna Sun, Jiwu Lou, Qiaoyi Li, Jianhong Chen, Yujuan Li, Dongzhi Li, Haiming Yuan, Yanhui Liu

    Published 2019
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  2. 42
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    Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction by Chih-Ping Chen, Tsang-Ming Ko, Wen-Chu Huang, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Chen-Wen Pan, Chien-Wen Yang, Wayseen Wang

    Published 2016
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  3. 43
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    A mesenteric primary peripheral Ewing's sarcoma/primitive neuroectodermal tumor with molecular cytogenetic analysis: Report of a rare case and review of literature by Yi-Shu Liao, I-Han Chiang, Hong-Wei Gao

    Published 2018
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  4. 44
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    Prenatal diagnosis and molecular cytogenetic characterization of inherited chromosome 2q11.1q11.2 microduplication with fetal intrauterine growth retardation by Yan Ma, E. Lei, Yunfan Xu, Yuexiang Feng

    Published 2022
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  5. 45
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    Prenatal diagnosis and molecular cytogenetic characterization of a pure ring chromosome 21 with a 4.657-Mb 21q22.3 deletion by Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Dai-Dyi Town, Wayseen Wang

    Published 2021
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  6. 46
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    Molecular cytogenetic characterization of isolated recurrent 4q35.2 microduplication in Chinese population: a seven-year single-center retrospective study by Jianlong Zhuang, Qiulan Wei, Yuying Jiang, Shuhong Zeng, Haijuan Lou, Na Zhang, Chunnuan Chen

    Published 2024
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  7. 47
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    Molecular cytogenetic characterization of 2q deletion and Xq duplication associated with nasal bone dysplasia in prenatal diagnosis: A case report and literature review by Mei-Ling Sun, Fa-Gui Yue, Xin-Yue Zhang, Yu-Ting Jiang, Lei-Lei Li, Hong-Guo Zhang, Rui-Zhi Liu

    Published 2022
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  8. 48
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    Clinical and Molecular Cytogenetic Characterisation of Children with Developmental Delay and Dysmorphic Features / Klinična in Molekularna Citogenetska Obravnava Otrok Z Razvojnim Zaostankom in Displastičnimi Znaki by Bertok Sara, Žerjav Tanšek Mojca, Kotnik Primož, Battelino Tadej, Volk Marija, Pecile Vanna, Cleva Lisa, Gasparini Paolo, Kovač Jernej, Hovnik Tinka

    Published 2015
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  9. 49
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    Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 associated with congenital hypoplasia of the tongue and review of the literature by Hui-Yuan Shao, Zong-Yu Miao, Xiao-Yan Liu, Xiao-Fei Hou, Hong Wu

    Published 2020
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  10. 50
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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 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

    Published 2020
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  11. 51
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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

    Published 2021
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  12. 52
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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

    Published 2017
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  13. 53
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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

    Published 2011
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  14. 54
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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

    Published 2011
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  15. 55
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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

    Published 2017
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  16. 56
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    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

    Published 2017
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  17. 57
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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

    Published 2019
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  18. 58
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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

    Published 2011
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  19. 59
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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

    Published 2011
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  20. 60
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    Prenatal diagnosis and molecular cytogenetic characterization of a de novo 3.19-Mb chromosome 14q32.13-q32.2 deletion of paternal origin by Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Wen-Lin Chen, Li-Feng Chen, Wayseen Wang

    Published 2020
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