Investigating CFTR gene variations in patient groups with positive newborn screening test results and preliminary clinical diagnosis of cystic fibrosis in the eastern anatolia regi... by Ayberk Turkyilmaz, Oguzhan Yarali

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Differential Diagnosis of Acromegaly: Pachydermoperiostosis Two New Cases from Turkey by Emine Kartal Baykan, Ayberk Türkyılmaz

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A Genetic Approach in the Evaluation of Short Stature by Ayberk Turkyilmaz, Ayse Sena Donmez, Atilla Cayir

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Genetic Forms of Calciopenic Rickets by Ayse Sena Donmez, Ayberk Turkyilmaz, Atilla Cayir

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Screening of MC4R, LEP, LEPR, POMC, SH2B1, and SIM1 genes in Turkish children with severe early-onset obesity by Ayberk Turkyilmaz, Oguzhan Yarali, Erdal Kurnaz, Atilla Cayir

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Prediction of molecular phenotypes for novel SCN1A variants from a Turkish genetic epilepsy syndromes cohort and report of two new patients with recessive Dravet syndrome by Kerem Teralı, Ayberk Türkyılmaz, Safiye Güneş Sağer, Alper Han Çebi

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Multigene Panel Testing in Turkish Hereditary Cancer Syndrome Patients by Esra ARSLAN ATES, Ayberk TURKYILMAZ, Ceren ALAVANDA, Ozlem YILDIRIM, Ahmet Ilter GUNEY

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NKX2-5 Gene Variants Associated with Congenital Heart Defects in Turkish Population by Bilgen Bilge Geçkinli, Gözde Girgin Özgümüş, Şenol Demir, Ayberk Türkyilmaz, Figen Akalın

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