Showing 1 - 4 results of 4 for search 'Dilek Doğruel', query time: 0.01s Refine Results
  1. 1
    Coexistence of 2 rare autosomal recessively inherited disorders manifesting with immune deficiency; IL-12 receptor β1 and biotinidase deficiencies

    Coexistence of 2 rare autosomal recessively inherited disorders manifesting with immune deficiency; IL-12 receptor β1 and biotinidase deficiencies by Dilek Doğruel, Fatma Derya Bulut, Mustafa Yılmaz, Neslihan Önenli-Mungan, Derya Ufuk Altıntaş

    Published 2018-10-01
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  2. 2
    Unusual and early onset IPEX syndrome: a case report

    Unusual and early onset IPEX syndrome: a case report by Dilek Doğruel, Fatih Gürbüz, İhsan Turan, Derya Ufuk Altıntaş, Mustafa Yılmaz, Bilgin Yüksel

    Published 2019-08-01
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  3. 3
    Clinical findings and genetic analysis of the patients with IL-12Rβ1 deficiency from southeast Turkey

    Clinical findings and genetic analysis of the patients with IL-12Rβ1 deficiency from southeast Turkey by Dilek Doğruel, Özlem Özgür Gündeşlioğlu, Mustafa Yılmaz, Derya Alabaz, Derya Ufuk Altıntaş, Emine Kocabaş

    Published 2019-04-01
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  4. 4
    Two years of newborn screening for cystic fibrosis in Turkey: Çukurova experience

    Two years of newborn screening for cystic fibrosis in Turkey: Çukurova experience by Ayşe Şenay Şaşihüseyinoğlu, Derya Ufuk Altıntaş, Atıl Bişgin, Dilek Doğruel, Mustafa Yılmaz, Mahir Serbes

    Published 2019-08-01
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