Presentation, Diagnosis, and Follow-Up Characteristics of 17α-Hydroxylase Deficiency Cases with Exon 1-6 Deletion (Founder Mutation) in the CYP17A1Gene: 20-Year Single-Center Experience.

Dundar İ., Akinci A., Camtosun E., Ciftci N., Kayas L.

Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation, cilt.17, sa.1, ss.43-50, 2023 (SCI-Expanded, Scopus)