Epilepsi ve anlıksal yetiyitimi olan hastalarda moleküler karyotiplemenin klinik yararı by Atıl BİŞGİN, Sevcan TUĞ BOZDOĞAN

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Nadir görülen iki genetik bozukluğun bir arada bulunması: bir çocukta kistik fibroz ve subkortikal kistleri olan megalensefalik lökoensefalopati by Faruk INCECİK, Mustafa YILMAZ, Atıl BİŞGİN

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Mitochondrial membrane protein–associated neurodegeneration: A case series of six children by Faruk Incecik, Ozlem M Herguner, Atil Bisgin

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Tıbbi genetik uygulamalarında altın standart fenomiks: tüm ekzom analizi yapılan 3 nörogenetik hasta örneği by Sevcan Tuğ Bozdoğan, Ibrahım Boga, Atıl Bişgin

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Identification of a novel homozygous variant in the alkaline phosphate (ALPL) gene associated with hypophosphatasia by Atil Bisgin, Ibrahim Boga, Cihan Cetin, Selim Buyukkurt

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IL-8, IL-10, TGF-β, and GCSF Levels Were Increased in Severe Persistent Allergic Asthma Patients with the Anti-IgE Treatment by Arzu D. Yalcin, Atil Bisgin, Reginald M. Gorczynski

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The impact of rare and low-frequency genetic variants in common variable immunodeficiency (CVID) by Atil Bisgin, Ozge Sonmezler, Ibrahim Boga, Mustafa Yilmaz

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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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Serum lubricin levels in patients with juvenile idiopathic arthritis by Rabia Miray Kisla Ekinci, Sibel Balcı, Fatma Coban, Atıl Bisgin

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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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Familial hypertrophic cardiomyopathy: A case with a new mutation in the MYBPC3 gene by Olgu Hallioglu Kilinc, Dilek Giray, Atil Bisgin, Sevcan Tug Bozdogan, Derya Karpuz

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The contribution of diet preference to the disease course in children with familial Mediterranean fever: a cross-sectional study by Rabia Miray Kisla Ekinci, Sibel Balcı, Atıl Bisgin, Fatma Cetin, Gokhan Tumgor

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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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Konjenital glukoz galaktoz malabsorbsiyonu sendromunda yeni bir mutasyon by Mehmet Satar, Mustafa Akçalı, Hacer Yapıcıoğlu Yıldızdaş, Ferda Özlü, Mehmet Ağın, Gökhan Tümgör, Atıl Bişgin

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Different clinical manifestations of three prime repair exonuclease 1 mutation: A case series by Faruk Incecik, Sibel Balci, Rabia Miray Kisla Ekinci, Ozlem M Herguner, Atil Bisgin, Mustafa Yilmaz

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Autosomal Dominant Polycystic Disease is Associated with Depressed Levels of Soluble Tumor Necrosis Factor-Related Apoptosis-Inducing Ligand by Funda Sarı, Arzu Didem Yalçın, Gizem Esra Genç, Metin Sarıkaya, Atıl Bisgin, Ramazan Çetinkaya, Saadet Gümüşlü

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Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in GALNT3 Gene: Experience from Southern Turkey by Rabia Miray Kışla Ekinci, Fatih Gürbüz, Sibel Balcı, Atıl Bişgin, Mehmet Taştan, Bilgin Yüksel, Mustafa Yılmaz

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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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Henoch Schönlein Purpurası tanılı çocuklarda Kompleman C2 gen polimorfizmleri by Rabia Miray KİSLA EKİNCİ, Sibel BALCİ, Bahriye ATMİS, Aysun KARABAY BAYAZİT, Dilek DOGRUEL, Derya Ufuk ALTİNTAS, Atil BİSGİN

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An Updated Review on the Role of Nanoformulated Phytochemicals in Colorectal Cancer by Alakesh Das, Suman Adhikari, Dikshita Deka, Nabajyoti Baildya, Padmavati Sahare, Antara Banerjee, Sujay Paul, Atil Bisgin, Surajit Pathak

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