يعرض 1 - 2 نتائج من 2 نتيجة بحث عن '"Cassa, C.A."', وقت الاستعلام: 1.44s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Inherited chst11/mir3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease

    المؤلفون: Chopra, S.S., Leshchiner, I., Duzkale, H., McLaughlin, H., Giovanni, M., Zhang, C., Cassa, C.A.

    المساهمون: Chopra, S.S., Leshchiner, I., Duzkale, H., McLaughlin, H., Giovanni, M., Zhang, C., Cassa, C.A., Yeditepe Üniversitesi

    مصطلحات موضوعية: CHST11, Inherited lymphoproliferative disorder, Malignant lymphoproliferative disorder, MIR3922, Skeletal malformation

    العلاقة: Molecular Genetics and Genomic Medicine; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; 413; 423; https://hdl.handle.net/20.500.11831/1568Test

    الإتاحة: https://doi.org/20.500.11831/1568Test
    https://hdl.handle.net/20.500.11831/1568Test

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  2. 2
    Inherited chst11/mir3922 deletion is associated with a novel recessive syndrome presenting with skeletal malformation and malignant lymphoproliferative disease

    المؤلفون: Chopra, SS, Leshchiner, I, Duzkale, H, McLaughlin, H, Giovanni, M, Zhang, CS, Cassa, CA

    المساهمون: Chopra, S.S., Leshchiner, I., Duzkale, H., McLaughlin, H., Giovanni, M., Zhang, C., Cassa, C.A., Yeditepe Üniversitesi, Chopra, SS, Leshchiner, I, Duzkale, H, McLaughlin, H, Giovanni, M, Zhang, CS, Cassa, CA

    مصطلحات موضوعية: Malignant lymphoproliferative disorder, CHST11, MIR3922, Skeletal malformation, Inherited lymphoproliferative disorder

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::747f31523dd923944d98cf63678f7456Test
    https://hdl.handle.net/20.500.11831/1568Test


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