IL7R GEN MUTASYON VE POLİMORFİZMLARİNİN AĞIR KOMBİNE İMMUN YETMEZLİKLİ HASTALARDAKİ SIKLIĞI by Derya Ufuk Altıntaş, Mustafa Yılmaz, İbrahim Boğa, Atıl Bişgin

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Renal features of Bardet Biedl syndrome: A single center experience by Bahriye Atmış, Aysun Karabay-Bayazıt, Engin Melek, Atıl Bişgin, Ali Anarat

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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

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Concomitance of Familial Mediterranean Fever and Gitelman syndrome in an adolescent by Bahriye Atmış, Rabia Miray Kışla-Ekinci, Engin Melek, Atıl Bişgin, Mustafa Yılmaz, Ali Anarat, Aysun Karabay-Bayazıt

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Evaluation of Patients Diagnosed with Congenital Glycosylation Defects: A Rainbow of Inherited Metabolic Disorders by Sebile Kılavuz, Fatma Derya Bulut, Deniz Kor, Berna Şeker Yılmaz, Atıl Bişgin, Fadli Demir, Bahriye Atmış, Derya Alabaz, Neslihan Mungan, Mustafa Yılmaz

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Clinical and laboratory aspects of patients diagnosed with various inherited platelet disorders by Veysel Gök, Alper Ozcan, Fatma Türkan Mutlu, Ebru Yılmaz, Deniz Kocak Göl, Mustafa Ozay, Baver Demir, Hüseyin Taskiran, Hasan Bas, Mehmet Burak Mutlu, Muhammet Ensar Dogan, Atil Bisgin, Ido Somekh, Meino Rohlfs, Munis Dundar, Yusuf Ozkul, Christoph Klein, Musa Karakukcu, Ekrem Unal

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