يعرض 1 - 4 نتائج من 4 نتيجة بحث عن '"Alpha globulin deletion"', وقت الاستعلام: 0.59s تنقيح النتائج
  1. 1
    دورية أكاديمية
    Asymptomatic hemochromatosis case with HFE c.1007−47G>A, c.340+4T>C heterozygous mutations and alpha globin −3.7 kb deletion

    المؤلفون: Akar, Nejat, Çelik, Vesile Deniz, Kılıç, Betül Orhan, ArdıçoÄŸlu Akışın, Nazife Yasemin

    مصطلحات موضوعية: Hemochromatosis, HFE gene mutation, Alpha globulin deletion

    العلاقة: Egyptian Journal of Medical Human Genetics; Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı; 110-8630; https://doi.org/10.1016/j.ejmhg.2018.06.001Test; https://hdl.handle.net/20.500.11851/3219Test; https://www.sciencedirect.com/science/article/pii/S1110863018300685Test; 19; 433; 435; 2-s2.0-85053318522; Q4

    الإتاحة: https://doi.org/20.500.11851/321910.1016/j.ejmhg.2018.06.001Test
    https://hdl.handle.net/20.500.11851/3219Test
    https://www.sciencedirect.com/science/article/pii/S1110863018300685Test

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  2. 2
    دورية أكاديمية
    Asymptomatic hemochromatosis case with HFE c.1007-47G>A, c.340+4T>C heterozygous mutations and alpha globin -3.7 kb deletion

    المؤلفون: Çelik, Vesile Deniz, Kiliç, Betul Orhan, Ardıçoğlu Akışin, Yasemin, Tükün, Fatma Ajlan, Akar, Nejat

    المصدر: Egyptian Journal of Medical Human Genetics; Vol 19, No 4 (2018); 433-435 ; 1110-8630

    مصطلحات موضوعية: Hemochromatosis, HFE gene mutation, Alpha globulin deletion

    وصف الملف: application/pdf

    العلاقة: https://www.ajol.info/index.php/ejhg/article/view/181817/171203Test; https://www.ajol.info/index.php/ejhg/article/view/181817Test

    الإتاحة: https://www.ajol.info/index.php/ejhg/article/view/181817Test

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  3. 3
    Asymptomatic hemochromatosis case with HFE c.1007−47G>A, c.340+4T>C heterozygous mutations and alpha globin −3.7 kb deletion

    مصطلحات موضوعية: Hemochromatosis, HFE gene mutation, Alpha globulin deletion

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=dris___02022::cb66520b6850d18a8dc1d2fd3c34d181Test
    https://hdl.handle.net/20.500.11851/797Test


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  4. 4
    Asymptomatic hemochromatosis case with HFE c.1007?47G>A, c.340+4T>C heterozygous mutations and alpha globin ?3.7?kb deletion

    المؤلفون: Yasemin Ardicoglu Akisin, Nejat Akar, Fatma Ajlan Tükün, Vesile Deniz Çelik, Betul Orhan Kiliç

    المساهمون: TOBB ETÜ, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, TOBB ETU, Faculty of Medicine, Department of Internal Medical Sciences, Çelik, Vesile Deniz, Kılıç, Betül Orhan, Akışın,Yasemin Ardıçoğlu, Akar, Nejat, TOBB ETU, Faculty of Medicine, Department of Basic Medical Sciences, TOBB ETÜ, Tıp Fakültesi, Temel Tıp Bilimleri Bölümü, Akışın, Yasemin Ardıçoğlu

    المصدر: Egyptian Journal of Medical Human Genetics, Vol 19, Iss 4, Pp 433-435 (2018)

    مصطلحات موضوعية: 0301 basic medicine, medicine.medical_specialty, lcsh:QH426-470, Thalassemia, Mean corpuscular hemoglobin, Alpha globulin deletion, Asymptomatic, Gastroenterology, 03 medical and health sciences, Internal medicine, medicine, Mean corpuscular volume, Genetics (clinical), Hemochromatosis, lcsh:R5-920, medicine.diagnostic_test, biology, business.industry, medicine.disease, Ferritin, lcsh:Genetics, 030104 developmental biology, Hereditary hemochromatosis, biology.protein, Hemoglobin, HFE gene mutation, medicine.symptom, lcsh:Medicine (General), business

    وصف الملف: application/pdf

    الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69470d1f99bdfe7e60f1b80512ab5a20Test
    https://doi.org/10.1016/j.ejmhg.2018.06.001Test


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