Search Results - "cytogenetics"

Immunophenotypes, cytogenetics, mutation profile of pediatric acute lymphoblastic leukemia: A retrospective study from tertiary care centre of Kashmir by Faisal Guru, Syed Nisar Ahmad, Mir Hussain, Ulfat Ara, Bashir Ahmad Charoo

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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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Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaic trisomy 12 at amniocentesis associated with a favorable pregnancy outcome by Chih-Ping Chen, Chen-Ju Lin, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Wen Pan, Chien-Wen Yang, Wayseen Wang

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Cytogenetic discrepancy between cultured amniocytes and uncultured amniocytes in mosaic trisomy 20 at amniocentesis in a pregnancy with a favorable outcome by Chih-Ping Chen, Yi-Hui Lin, Peih-Shan Wu, Schu-Rern Chern, Shin-Wen Chen, Fang-Tzu Wu, Chen-Chi Lee, Chen-Wen Pan, Yun-Yi Chen, Wayseen Wang

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Mosaicism for trisomy 2 in a single colony at amniocentesis in a pregnancy with a favorable outcome and cytogenetic discrepancy at different amniocenteses by Chih-Ping Chen

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Detection of cytogenetic changes and chromosomal aneuploidy with fluorescent in situ hybridization in cytological specimens of oral cancers in Fanconi anemia-Proof of concept by Bruno Eduardo Silva de Araujo, Eunike Velleuer, Ralf Dietrich, Natalia Pomjanski, Isabela Karoline deSantana Almeida Araujo, Martin Schlensog, Susanne Irmtraud Wells, Josephine Christine Dorsman, Martin Schramm

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Multiple Myeloma Patients at Various Cytogenetic Risks Benefit Differently from Autologous Stem Cell Transplantation as a Consolidation Therapy by Tianmei Zeng, Lili Zhou, Hao Xi, Weijun Fu, Juan Du, Chunyang Zhang, Hua Jiang, Jian Hou

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Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 4 by Chih-Ping Chen, Ming Chen, Yi-Ning Su, Fuu-Jen Tsai, Schu-Rern Chern, Pei-Chen Wu, Wen-Lin Chen, Li-Feng Chen, Chen-Wen Pan, Wayseen Wang

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Molecular cytogenetic characterization of 16p11.2 microdeletions with diverse prenatal phenotypes: Four cases report and literature review by Fagui Yue, Qi Xi, Xinyue Zhang, Yuting Jiang, Hongguo Zhang, Ruizhi Liu

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Assessment of fibrosis and vascularization of bone marrow stroma of chronic myeloid Leukemia patients treated with imatinib mesylate and their relationship with the cytogenetic response by Caroline Regina de Jesus, Lee I-Ching, Teresinha de Jesus Carvalho Neiva, Cidônia de Lourdes Vituri

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Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2 by Chih-Ping Chen, Ming Chen, Schu-Rern Chern, Peih-Shan Wu, Shun-Ping Chang, Dong-Jay Lee, Yu-Ting Chen, Li-Feng Chen, Jun-Wei Su, Alan Hwa-Ruey Hsieh, Alex Hwa-Jiun Hsieh, 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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A cytogenetically cryptic case of otherwise obvious acute promyelocytic leukemia: The importance of real time RT-PCR molecular analysis by Keegan Barry-Holson, David Steiner, Scott Wendroth, Athena Cherry, James L. Zehnder, Robert S. Ohgami

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Pallister-Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes.... by Francesco Libotte, Domenico Bizzoco, Ivan Gabrielli, Alvaro Mesoraca, Pietro Cignini, Salvatore Giovanni Vitale, Ilaria Marilli, Ferdinando Antonio Gulino, Agnese Maria Chiara Rapisarda, Claudio Giorlandino

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Meiosis Molecular Mechanisms and Cytogenetic Diversity

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Clinical and molecular cytogenetic findings of cat eye syndrome and a 2-year-old patient with congenital aural atresia and hearing loss by Liang Xu, Xia Cheng, Lemin Tang, Shengping Min, Jiatao Wu, Hongwei Zhu, Yaping Liao

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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 Chih-Ping Chen, Tsang-Ming Ko, Yi-Yung Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Chien-Wen Yang, Chen-Wen Pan, 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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Directly transmitted 4.5-Mb triplication of 4q12-q13.1: Prenatal diagnosis and molecular cytogenetic characterization by Chih-Ping Chen, Ming-Huei Lin, Schu-Rern Chern, Yu-Ting Chen, Peih-Shan Wu, Yu-Ling Kuo, Meng-Shan Lee, Wayseen Wang

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Low-level mosaic trisomy 13 at amniocentesis in a pregnancy associated with a favorable fetal outcome and cytogenetic discrepancy in various tissues by Chih-Ping Chen, Shun-Long Weng, Shin-Wen Chen, Schu-Rern Chern, Peih-Shan Wu, Fang-Tzu Wu, Yen-Ting Pan, Chen-Chi Lee, Wen-Lin Chen, Wayseen Wang

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