Search Results - "cytogenetics"

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  1. 641
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    Prenatal diagnosis of a fetus with mosaic ring chromosome 13: Case report and review of the literature by Xiao-Nan Hu, Lei-Lei Li, Qing-Yang Shi, Zhu-Ming Hu, Hong-Guo Zhang, Yu-Ting Jiang, Rui-Zhi Liu

    Published 2021
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  2. 642
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    Prenatal diagnosis by whole exome sequencing in a family with a novel TBR1 mutation causing intellectual disability by Chunyan Jin, Hua Qian, Tianhui Xu, Jiao Chen, Xuefang Li, Zhiping Gu

    Published 2021
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  3. 643
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    Cutaneous Epithelioid Clear Cells Angiosarcoma in a Young Woman with Congenital Lymphedema by Flore Tabareau-Delalande, Anne de Muret, Elodie Miquelestorena-Standley, Anne-Valérie Decouvelaere, Gonzague de Pinieux

    Published 2013
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  4. 644
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    Targeted Therapies for Pediatric AML: Gaps and Perspective by Annalisa Lonetti, Andrea Pession, Andrea Pession, Riccardo Masetti

    Published 2019
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  5. 645
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    Clinical Impact of Genomic Information in Pediatric Leukemia by Emilie Lalonde, Gerald Wertheim, Marilyn M. Li, Marilyn M. Li

    Published 2017
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  6. 646
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    Complex karyotype in myelodysplastic syndromes: Diagnostic procedure and prognostic susceptibility by Mohammad Shahjahani, Elham Homaei Hadad, Shirin Azizidoost, Kowsar Chenani Nezhad, Saeid Shahrabi

    Published 2019
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  7. 647
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    Metastatic renal cell carcinoma - a case report by Grzegorz Wróbel

    Published 2017
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  8. 648
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    The role of dasatinib in the management of chronic myeloid leukemia by Chen R, Chen B

    Published 2015
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  9. 649
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    Insights from Animal Reproduction

    Published 2016
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  10. 650
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    Familial Translocation (2;18) Ascertained Through Recurrent Spontaneous Abortions by Gülseren Bağcı, Emre Tepeli, Füsun Düzcan, Ozan Çetin, Erkan Alataş

    Published 2010
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  11. 651
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    Hepatic myeloid sarcoma preceding acute megakaryoblastic leukemia with t(1;22) in an infant: Case report by Zeynep Canan Özdemir, Ayşe Bozkurt Turhan, Beyhan Durak Aras, Berat Acu, Özcan Bör

    Published 2016
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  12. 652
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    Lack of MDM2 interpretation guidelines contribute to diagnostic difficulty in a case of undifferentiated sarcoma by Melissa M. Straub, Ferrin C. Wheeler, Sarah M. Deraney, Emily S. Reisenbichler

    Published 2018
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  13. 653
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    A novel phenotype of 13q12.3 microdeletion characterized by epilepsy in an Asian child: a case report by Mina Wang, Bin Li, Zehuan Liao, Yu Jia, Yuanbo Fu

    Published 2020
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  14. 654
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    SATB2 gene variants in non-syndromic cleft lip with or without cleft palate in Indian population by Venkatesh Babu Gurramkonda, Altaf Hussain Syed, Jyotsna Murthy, Bhaskar V.K.S. Lakkakula

    Published 2015
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  15. 655
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    Your dilemma, my identity: Unusual immunogenetic profiles of pediatric B cell acute lymphoblastic leukemia by Anurag Gupta, Manu Goyal, Koteswara Rao Nidamanuri, Palanki Satya Dattatreya

    Published 2014
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  16. 656
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    Prenatal diagnosis of Pallister-Killian syndrome in pregnancy with normal CVS result and abnormal ultrasound findings in the second trimester by Veronika Frisova, Ivana Tutkova Svobodova, Michaela Tozzi, Dagmar Raskova

    Published 2018
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  17. 657
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    Therapy related myelodysplastic syndrome: A case report and review of literature by Smita Sonawane, Nitin Gadgil, Sangita Margam

    Published 2011
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  18. 658
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    Prenatal Diagnosis of WAGR Syndrome by Berrin Tezcan, Philip Rich, Amarnath Bhide

    Published 2015
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  19. 659
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    Prenatal diagnosis of partial monosomy 21q (21q22.1→qter) associated with intrauterine growth restriction and corpus callosum dysgenesis by Ying-Chung Chen, Wan-Ju Wu, Shun-Ping Chang, Gwo-Chin Ma, Ming Chen

    Published 2020
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  20. 660
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    Non-Mosaic Tetrasomy 9p in An Infant With Multiple Congenital Anomalies by Füsun Düzcan, Hacer Ergin, Melike Aytan, Emre Tepeli, Özmert Özdemir, Seher Başaran

    Published 2007
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