The Turkish Journal of Pediatrics 2020 , Vol 62 , Num 5
Atypical presentation in patients with 17 α-hydroxylase deficiency caused by a deletion in the CYP17A1 gene: short stature
Semih Bolu 1 ,Recep Eröz 2 ,Mehmet Tekin 3 ,Mustafa Doğan 2
1 Division of Pediatric Endocrinology, Adıyaman University Faculty of Medicine, Adıyaman, Turkey
2 Department of Medical Genetics, Düzce University Faculty of Medicine, Düzce, Turkey
3 Department of Pediatrics, Adıyaman University Faculty of Medicine, Adıyaman, Turkey
DOI : 10.24953/turkjped.2020.05.019 Keywords :
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