Search Results - "cytogenetics"

Down Syndrome Due to Unbalanced Homologous Acrocentric Rearrangements and its Recurrence in Subsequent Pregnancies: Prenatal Diagnosis by Amniocentesis by Chih-Ping Chen, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Shu-Shien Chiang, Chen-Chi Lee, Wayseen Wang

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The correlation between micronuclei count and smoking behavior: A hospital-based study by Lakshmi Balraj, UnniKrishnan K, Tejavathi Nagaraj

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Genetic Causes of Mental Retardation in Golestan Province by Hossein Darvish, Saghar Ghasemi-Firouzabadi, Gholam Reza Bahrami-Monajemi, Ideh Bahman, Marziyeh Mohseni, Mohammad Javad Soltani-Banavandi, Sousan Banihashemi , Sanaz Arjangi, Farkhondeh Behjati, Kimia Kahrizi, Hossein Najmabadi

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A case of Roberts syndrome: its ultrasonographic characteristics and genetic diagnosis by Ayaz, Reyhan, Göktaş, Emine, Balasar, Mine

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Molecular delineation of de novo small supernumerary marker chromosomes in prenatal diagnosis, a retrospective study by Shuang Hu, Xiangdong Kong

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Management of Amniocentesis in High Risk Pregnancies and The Evaluation of the Results by Osman Balcı, Ali Acar, Metin Çapar, Cemalettin Akyürek, Gül Durakbaşı, Ayşegül Zamani, Aynur Acar

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Chromosome aberrations, valued as frequency of spontaneous micronuclei, in subjects with suspected presclerodermic Raynaud's phenomenon by G. Porciello, R. Scarpato, F. Storino, F. Cagetti, F. Bellisai, G. Morozzi, R. Marcolongo, L. Migliore, C. Ferri, M. Galeazzi

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A STUDY ON THE ROLE OF THE RB1 GENE AS A PROGNOSTIC FACTOR IN UNTREATED PATIENTS WITH B-CHRONIC LYMPHOCYTIC LEUKEMIA by Vanya Slavcheva, Svetlana Angelova, Georgi Balatzenko, Tzvetan Lukanov, Pencho Tonchev

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Therapy-Induced Neural Differentiation in Ewing's Sarcoma: A Case Report and Review of the Literature by Kıvılcım Eren ERDOĞAN, Mehmet Ali DEVECİ, Zeynep Ruken HAKKOYMAZ, Gülfiliz GÖNLÜŞEN

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Prenatal Diagnosis of mos45,X/46,X,+mar in a Fetus With Normal Male External Genitalia and a Literature Review by Shu-Chin Chien, Chih-Ping Chen, Chyi-Chyang Lin, Li-Chia Huang, Cheng-Tiao Hsieh, Fuu-Jen Tsai

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Lenalidomide as potential treatment in small cell neuroendocrine lung cancer with del 5q by Paul Hartel

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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 Chih-Ping Chen, Tsang-Ming Ko, Jian-Pei Huang, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Wen-Lin Chen, Meng-Shan Lee, Wayseen Wang

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Chondromyxoid fibroma of rib with a novel chromosomal translocation: a report of four additional cases at unusual sites by Parwani Anil V, Surti Urvashi, Gollin Susanne M, Goodman Mark A, McGough Richard L, Armah Henry B, Rao Uma NM

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Survival and Prognostic Factors in Adults Acute Myeloid Leukemia: A Retrospective Analysis of 119 Cases by Alina Maria Gridjac, Cristian Daniel Pirlog, Anca Simona Bojan

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Gestational, perinatal and family findings of patients with Patau syndrome by Rafael Fabiano M. Rosa, Melina Vaz Sarmento, Janaina Borges Polli, Daniela de Paoli Groff, Patrícia Petry, Vinícius Freitas de Mattos, Rosana Cardoso M. Rosa, Patrícia Trevisan, Paulo Ricardo G. Zen

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Survival and Prognostic Factors in Adults Acute Myeloid Leukemia: A Retrospective Analysis of 119 Cases by Alina M Gridjac, Cristian Daniel Pirlog, Anca Simona Bojan

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Evaluation of Cytotoxic and Genotoxic Effects in Buccal Mucosal Cells in Non-Smokers and Users of Traditional Combustible Tobacco Products and Non-Combustible Alternatives by Antonija Tadin, Vinka Stazic, Nada Galic, Davor Zeljezic

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Evaluation of the CD123 Expression and FLT3 Gene Mutations in Patients with Acute Myeloid Leukemia by Freidoon Solhjoo, Akbar Safaie, Ahmad Monabati, Maral Mokhtari, Moeinadin Safavi

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15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review by Yahya Benbouchta, Nicole De Leeuw, Saadia Amasdl, Aziza Sbiti, Dominique Smeets, Khalid Sadki, Abdelaziz Sefiani

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Classification of human cancers based on DNA copy number amplification modeling by Knuutila Sakari, Böhling Tom, Tikka Jarkko, Myllykangas Samuel, Hollmén Jaakko

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