Search Results - "cytogenetics"

Prenatal diagnosis of low-level mosaic trisomy 20 by amniocentesis in a pregnancy with a favorable outcome by Chih-Ping Chen, Yu-Ling Kuo, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Li-Feng Chen, Wayseen Wang

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Effect of a homeopathic drug, Chelidonium, in amelioration of p-DAB induced hepatocarcinogenesis in mice by Khuda-Bukhsh Anisur, Biswas Surjyo

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Additional evidence for the role of chromosomal imbalances and SOX8, ZNRF3 and HHAT gene variants in early human testis development by Khouloud Rjiba, Soumaya Mougou-Zerelli, Imen hadj Hamida, Ghada Saad, Bochra Khadija, Afef Jelloul, Wafa Slimani, Yosra Hasni, Sarra Dimassi, Hela Ben khelifa, Amira Sallem, Molka Kammoun, Hamza Hadj Abdallah, Moez Gribaa, Joelle Bignon-Topalovic, Sami Chelly, Hédi Khairi, Mohamed Bibi, Maha Kacem, Ali Saad, Anu Bashamboo, Kenneth McElreavey

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A 46,XX karyotype in men with infertility: Two new cases and review of the literature by Elisavet Kouvidi, Hara Tsimela, Leandros Lazaros, Kalliopi N Manola, Sophia Zachaki, Ruxandra Dobrescu, Konstantinos Sfakianoudis, Theodora Tsoni, Christina Katsidi, Haralambia Tsarouha, Emmanuel Kanavakis, Ariadni Mavrou

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Detection of mosaic 15q11.1-q11.2 deletion encompassing NBEAP1 and POTEB in a fetus with diffuse lymphangiomatosis by Chih-Ping Chen, Kuo-Gon Wang, Hsu-Kuang Huang, Cheng-Ran Peng, Schu-Rern Chern, Peih-Shan Wu, Yen-Ni Chen, Shin-Wen Chen, Chen-Chi Lee, Wayseen Wang

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De novo duplication of Xq22.1→q24 with a disruption of the NXF gene cluster in a mentally retarded woman with short stature and premature ovarian failure by Chih-Ping Chen, Yi-Ning Su, Hung-Hung Lin, Schu-Rern Chern, Fuu-Jen Tsai, Pei-Chen Wu, Chen-Chi Lee, Yu-Ting Chen, Wayseen Wang

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Application of clinical nomograms to predicting overall survival and event-free survival in multiple myeloma patients: Visualization tools for prognostic stratification by Jiaxuan Xu, Yifan Zuo, Jingjing Sun, Min Zhou, Xiaoqing Dong, Bing Chen

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Time to reduce the rate of idiopathic recurrent pregnancy losses by T. M. Tutchenko, O. A. Burka, V. S. Samilyk, O. V. Trokhymovych, O. I. Krotik, O. L. Gromova

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Phenotype to genotype characterization by array-comparative genomic hydridization (a-CGH) in case of fetal malformations: A systematic review by Gabriele Tonni, Marcella Palmisano, Ana Cristina Perez Zamarian, Ana Carolina Rabachini Caetano, Eduardo Félix Martins Santana, Alberto Borges Peixoto, Edecio Armbruster-Moraes, Rodrigo Ruano, Edward Araujo Júnior

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BURKITT'S LYMPHOMA WITH A PRIMARY LESION OF THE STOMACH (CLINICAL OBSERVATION) by A. O. Kasimova, Yu. D. Udalov, V. V. Korenkov, L. Yu. Ilchenko

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A female patient with retinoblastoma and severe intellectual disability carrying an X;13 balanced translocation without rearrangement in the RB1 gene: a case report by Makiko Tsutsumi, Hiroyoshi Hattori, Nobuhiro Akita, Naoko Maeda, Toshinobu Kubota, Keizo Horibe, Naoko Fujita, Miki Kawai, Yasuko Shinkai, Maki Kato, Takema Kato, Rie Kawamura, Fumihiko Suzuki, Hiroki Kurahashi

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Prenatal identification of partial 3q duplication syndrome by Magdalena Pasińska, Rafał Adamczak, Anna Repczyńska, Ewelina Łazarczyk, Barbara Iskra, Agata Klaudia Runge, Olga Haus

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Fragile X Syndrome by J Gordon Millichap

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Chromosomal Abnormalities in ADHD by J Gordon Millichap

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Angelman Syndrome: Chromosome Abnormality by J Gordon Millichap

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Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum by Chih-Ping Chen, Chin-Yuan Hsu, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Wayseen Wang

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Prenatal and Postnatal Diagnosis and Genetic Background of Corpus Callosum Malformations and Neonatal Follow-Up by Virág Bartek, István Szabó, Ágnes Harmath, Gábor Rudas, Tidhar Steiner, Attila Fintha, Nándor Ács, Artúr Beke

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Choroid Plexus Cysts: Single Nucleotide Polymorphism Array Analysis of Associated Genetic Anomalies and Resulting Obstetrical Outcomes by Cai M, Huang H, Su L, Wu X, Xie X, Xu L, Lin N

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G2/M Checkpoint Abrogation With Selective Inhibitors Results in Increased Chromatid Breaks and Radiosensitization of 82-6 hTERT and RPE Human Cells by Aggeliki Nikolakopoulou, Aggeliki Nikolakopoulou, Aashish Soni, Martha Habibi, Martha Habibi, Pantelis Karaiskos, Gabriel Pantelias, Georgia I. Terzoudi, George Iliakis

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Detection of recurrent 4p16.3 microdeletion with 2p25.3 microduplication by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in a fetus... by Wen-Xu Yang, Hong Pan, Song-Tao Wang, Lin Li, Hai-Rong Wu, Yu Qi

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