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, Ismail ; Akinci, Aysehan ; Camtosun, Emine ; Ciftci, Nurdan ; Kayas, Leman
Sexual development, 2023, Vol.17 (1), p.43-50 [Revista revisada por pares]Basel, Switzerland
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