Search Results - "cytogenetics"

Evaluation of micronuclei and antioxidant status in hospital radiation workers occupationally exposed to low-dose ionizing radiation by S. N. Mousavikia, M. T. Bahreyni Toossi, S. Khademi, M. Soukhtanloo, H. Azimian

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Application of omics in the diagnosis, prognosis, and treatment of acute myeloid leukemia by Zhiyu Zhang, Jiayi Huang, Zhibo Zhang, Hongjie Shen, Xiaowen Tang, Depei Wu, Xiebing Bao, Guoqiang Xu, Suning Chen

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CHROMOSOMAL ABNORMALITIES AND Y CHROMOSOME MICRODELETIONS IN BULGARIAN MALE WITH AZOOSPERMIA OR SEVERE OLIGOSPERMIA by Katya Kovacheva, Rumen Kotsev, Emiliana Konova, Violeta Rilcheva, Zornitsa Kamburova, Maria Simeonova

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Prenatal diagnosis of de novo small supernumerary marker chromosome 4q (4q11-q12): A case report by Reza Mohammadi, Raheleh Taheri, Fatemeh Shahriyari, Farnaz Feiz, Zahra Mohammadi, Sadegh Shirian, Reza Raoofian, Abdorrasoul Malekpour, Reza Pazhoomand

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The genomic and molecular landscape of splenic marginal zone lymphoma, biological and clinical implications by Amatta Mirandari, Helen Parker, Margaret Ashton-Key, Benjamin Stevens, Renata Walewska, Kostas Stamatopoulos, Dean Bryant, David G. Oscier, Jane Gibson, Jonathan C. Strefford

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Discordant Prenatal Cell-Free DNA Screening vs. Diagnostic Results of Sex Chromosome Aneuploidies: Implications for Newborn Screening and Genetic Counseling by Susan Howell, Shanlee M. Davis, Billie Carstens, Mary Haag, Judith L. Ross, Nicole R. Tartaglia

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Detection of Chromosome Aberrations in the Second Trimester Using Genetic Amniocentesis: Experience During 1995-2004 by Jenn-Jhy Tseng, Min-Min Chou, Feng-Chu Lo, Hui-Yu Lai, Min-Hui Chen, Esther Shih-Chu Ho

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Identification of a novel TP63 mutation causing nonsyndromic cleft lip with or without cleft palate by Tianhui Xu, Mengmeng Du, Xinhua Bu, Donglan Yuan, Zhiping Gu, Pei Yu, Xuefang Li, Jiao Chen, Chunyan Jin

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An Unusual Clinical and Radiological Presentation of Ovotesticular Disorders of Sex Development with Male and Female External Genitalia: A Case Report by Muhammad Tahir Khan, Abeer Yasin, Rewati Raman, Nighat Haroon Khan

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Prenatal diagnosis of mosaicism for a distal 5p deletion in a single colony at amniocentesis in a pregnancy with a favorable outcome and a review of mosaic distal 5p deletion by Chih-Ping Chen, Liang-Kai Wang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wen-Lin Chen, Wayseen Wang

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What's new in genetics of congenital heart defects by Maria Cristina Digilio, Bruno Marino

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PAH biomarkers for human health risk assessment: a review of the state-of-the-art Biomarcadores de HPAs na avaliação de risco à saúde humana: uma revisão do estado da arte... by Sérgio Silveira Franco, Adelaide Cássia Nardocci, Wanda Maria Risso Günther

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Comparison of micronuclei frequency between smokers and non-smokers: a systematic review by Rodrigo B Andrade, Nadine Alessandra Campos

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A 13-year-old girl with 18p deletion syndrome presenting Turner syndrome-like clinical features of short stature, short webbed neck, low posterior hair line, puffy eyelids and incr... by Chih-Ping Chen, Shuan-Pei Lin, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Shih-Ting Lai, Tzu-Yun Chuang, Wen-Lin Chen, Wayseen Wang

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Osteogenesis imperfecta type I: Second-trimester diagnosis and incidental identification of a dominant COL1A1 deletion mutation in the paucisymptomatic father by Chih-Ping Chen, Yi-Ning Su, Tung-Yao Chang, Schu-Rern Chern, Chen-Yu Chen, Jun-Wei Su, Wayseen Wang

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VACTERL association with hydrocephalus in a fetus conceived by in vitro fertilization and embryo transfer by Chih-Ping Chen, Tung-Yao Chang, Yi-Yung Chen, Schu-Rern Chern, Jun-Wei Su, Wayseen Wang

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The pyroptosis-related gene signature predicts prognosis and reveals characterization of the tumor immune microenvironment in acute myeloid leukemia by Tao Zhou, Tao Zhou, Kai Qian, Kai Qian, Yun-Yun Li, Wen-Ke Cai, Sun-Jun Yin, Ping Wang, Gong-Hao He, Gong-Hao He

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Deleção do cromossomo 9 na região q22q32 em bebê com cariótipo 46XY: relato de um caso Deletion of chromosome 9 in the region q22q32 in a male baby with karyotype 46XY: report... by Seme Youssef Reda, Jean Ricardo Nicareta

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A case of Ph+ acute lymphoblastic leukemia and EGFR mutant lung adenocarcinoma synchronous overlap: may one TKI drug solve two diseases? by Qi Zhang, Jing-dong Zhou, Hao Ding, Lei Yang, Chao Lu, Ming-qiang Chu, Jun Qian, Ting-juan Zhang

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An integrated linkage, chromosome, and genome map for the yellow fever mosquito Aedes aegypti. by Vladimir A Timoshevskiy, David W Severson, Becky S Debruyn, William C Black, Igor V Sharakhov, Maria V Sharakhova

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