Showing 1 - 11 results of 11 for search 'Zerrin Yilmaz', query time: 0.03s Refine Results
  1. 1
    Compound heterozygous Niemann-Pick Type C disease in the neonatal period

    Compound heterozygous Niemann-Pick Type C disease in the neonatal period by Özden Turan, Zerrin Yilmaz, Ayşe Ecevit, Deniz Anuk-ince

    Published 2021-09-01
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  2. 2
    Complex cytogenetic findings in the bone marrow of a chronic idiopathic myelofibrosis patient

    Complex cytogenetic findings in the bone marrow of a chronic idiopathic myelofibrosis patient by Tuğçe Bulakbaşı Balcı, Meltem Yüksel, Zerrin Yılmaz, Feride İffet Şahin

    Published 2010-06-01
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  3. 3
    Complex cytogenetic findings in the bone marrow of a chronic idiopathic myelofibrosis patient

    Complex cytogenetic findings in the bone marrow of a chronic idiopathic myelofibrosis patient by Tuğçe Bulakbaşı Balcı, Meltem Yüksel, Zerrin Yılmaz, Feride İffet Şahin

    Published 2010-06-01
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  4. 4
    Fluorescence in situ hybridization analysis of the hTERC region in acute myeloid leukemia patients

    Fluorescence in situ hybridization analysis of the hTERC region in acute myeloid leukemia patients by Özge Özer, Tuğçe Bulakbaşı Balcı, Zerrin Yılmaz, Feride İffet Şahin

    Published 2011-06-01
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  5. 5
    Fluorescence in situ hybridization analysis of the hTERC region in acute myeloid leukemia patients

    Fluorescence in situ hybridization analysis of the hTERC region in acute myeloid leukemia patients by Özge Özer, Tuğçe Bulakbaşı Balcı, Zerrin Yılmaz, Feride İffet Şahin

    Published 2011-05-01
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  6. 6
    Importance of Routine Ultrasonography in Detecting Fetal Karyotype Abnormalities in Low Risk Pregnancies

    Importance of Routine Ultrasonography in Detecting Fetal Karyotype Abnormalities in Low Risk Pregnancies by Zerrin Yılmaz, Özge Özer, Derya Eroğlu, Filiz Yanık, Feride İffet Şahin

    Published 2012-04-01
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  7. 7
    Blastoid Variant Mantle Cell Lymphoma with Complex Karyotype Including 11q Duplication

    Blastoid Variant Mantle Cell Lymphoma with Complex Karyotype Including 11q Duplication by Özge Özer, Selami K. Toprak, Enver Öte, Zerrin Yılmaz, Feride İffet Şahin

    Published 2014-08-01
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  8. 8
    İzole TB delesyonu saptanan 22q11 delesyon sendromlu bir yenidoğan olgusu

    İzole TB delesyonu saptanan 22q11 delesyon sendromlu bir yenidoğan olgusu by Özden TURAN, Zerrin YILMAZ ÇELİK, Deniz ANUK INCE, Yunus Kasım TERZİ, Ayşe ECEVİT

    Published 2020-03-01
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  9. 9
    22q13.3 Delesyon Sendromu: Mental Retardasyonun Az Tanınan Bir Nedeni

    22q13.3 Delesyon Sendromu: Mental Retardasyonun Az Tanınan Bir Nedeni by İlknur EROL, Özge SÜRMELİ ONAY, Zerrin YILMAZ, Özge ÖZER, Füsun ALEHAN, Feride ŞAHİN

    Published 2015-09-01
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  10. 10
    22q13.3 Deletion Syndrome: An Underdiagnosed Cause of Mental Retardation

    22q13.3 Deletion Syndrome: An Underdiagnosed Cause of Mental Retardation by ilknur Erol, Ozge Surmeli Onay, Zerrin Yilmaz, Ozge Ozer, Fusun Alehan, Feride iffet sahin

    Published 2015-03-01
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  11. 11
    Effect of Hereditary Hemochromatosis Gene H63D and C282Y Mutations on Iron Overload in Sickle Cell Disease Patients

    Effect of Hereditary Hemochromatosis Gene H63D and C282Y Mutations on Iron Overload in Sickle Cell Disease Patients by Yunus Kasım Terzi, Tuğçe Bulakbaşı Balcı, Can Boğa, Zafer Koç, Zerrin Yılmaz Çelik, Hakan Özdoğu, Sema Karakuş, Feride İffet Şahin

    Published 2016-11-01
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