Search Results - "cytogenetics"

Chromosomal microarrays testing in children with developmental disabilities and congenital anomalies by Guillermo Lay-Son, Karena Espinoza, Cecilia Vial, Juan C. Rivera, María L. Guzmán, Gabriela M. Repetto

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Plasma Proteins as Biomarkers of Mortality After Total Body Irradiation in Mice by Hanjiang Fu, Yong Xue, Fei Su, Kexin Ding, Yuan Wang, Haiyue Yu, Jie Zhu, Qing Li, Changhui Ge, Xiaofei Zheng

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Exome-First Approach in Fetal Akinesia Reveals Chromosome 1p36 Deletion Syndrome by Masatake Toshimitsu, Shinichi Nagaoka, Shuusaku Kobori, Maki Ogawa, Fumihiko Suzuki, Takema Kato, Shunsuke Miyai, Rie Kawamura, Hidehito Inagaki, Hiroki Kurahashi, Jun Murotsuki

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Primary plasma cell leukemia: A report of two cases of a rare and aggressive variant of plasma cell myeloma with the review of literature by Prithal Gangadhar, Zulfikar Ahmed, Muktha R Pai, I Sandhya

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Multiple Exposures and Coexposures to Occupational Hazards Among Agricultural Workers: A Systematic Review of Observational Studies by Thi-, Mélanie Bertin, Julie Bodin, Natacha Fouquet, Nathalie Bonvallot, Yves Roquelaure

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THE FINAL ANALYSIS: 10-YEAR TREATMENT RESULTS OF ACUTE LYMPHOBLASTIC LEUKEMIA IN CHILDREN OF SAINT-PETERSBURG ON THE PROTOCOL COALL-92-SAINT-PETERSBURG by E.G. Boichenko

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A Case of B-cell Precursor Acute Lymphoblastic Leukemia with the t(14;22)(q32;q11) Presenting Hyperleukocytosis by Jianne Lee, Sun Young Kim, Yeon Jung Lim

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A rare of Turner syndrome with a special karyotype: a case report by W.D. Huang, M. Pang, Q.Z. Zhao, X.P. Wang, J. Wang, Y. Mao, L.Y. Kong, B. Liang

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Factor VII deficiency and developmental abnormalities in a patient with partial monosomy of 13q and trisomy of 16p: case report and review of the literature by Meck Jeanne M, Brooks Brian P, Haddad Bassem R, Bendavid Claude, Blain Delphine, Toretsky Jeffrey A

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THE FINAL ANALYSIS: 10-YEAR TREATMENT RESULTS OF ACUTE LYMPHOBLASTIC LEUKEMIA IN CHILDREN OF SAINT-PETERSBURG ON THE PROTOCOL COALL-92-SAINT-PETERSBURG by E.G. Boichenko

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Tertiary care center experience: An overview of primary mediastinal lymphomas by Paheli Maru, Beena Brahmbhatt, Sangita Vanik, Sneha Kakoty

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Retinoblastoma tumor suppressor gene: An overview by Sunila Thomas, Anita Balan

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HUMAN GENETIC VARIANTS AND THEIR ANALYSIS: CURRENT STATE AND FUTURE PERSPECTIVES by Lara Slavec, Ksenija Geršak, Nataša Karas Kuželički, Katarina Trebušak Podkrajšek

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De novo chronic lymphocytic leukemia/prolymphocytic leukemia or B-cell prolymphocytic leukemia? The importance of integrating clinico-morphological and immunophenotypic findings in... by Zachariah Chowdhury, Yookarin Khonglah, Susmita Sarma, Pranjal Kalita

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A Chinese family with cat eye syndrome and abnormality of eye movement: First case report by Yang Lu, Liping Shen, Yue Zheng, Haichen Zhang, Yanbo Liu, Ming Qi, Ming Qi, Shangzhi Huang, Bo Shen

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Utility of Transmission Electron Microscopy in Small Round Cell Tumors by Na Rae Kim, Seung Yeon Ha, Hyun Yee Cho

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Novel balanced chromosomal translocations in females with recurrent spontaneous abortions: Two case studies by Puspal De, Sudipa Chakravarty, Amit Chakravarty

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Prenatal diagnosis of a familial 9p12 amplification inherited from a father carrier by Chih-Ping Chen, Chen-Yu Chen, Schu-Rern Chern, Peih-Shan Wu, Shin-Wen Chen, Fang-Tzu Wu, Yun-Yi Chen, Chen-Chi Lee, Chen-Wen Pan, Wayseen Wang

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Evaluation of Six Patients with Chromosome 18 Structural Anomalies and Novel Findings by Esra Işık, Bilcağ Akgün, Tahir Atik, Ferda Özkınay, Özgür Çoğulu

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Partial tetrasomy 18 mosaicism: Pre and postnatal diagnosis of a unique pattern by Telma Luís, Cristina Candeias, Sara Domingues, Natália Oliva-Teles, Céu Mota, Cláudia Falcão Reis

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