CYP21 Gene Mutations in Congenital Adrenal Hyperplasia due To 21-Hydroxylase Deficiency: Genotype-Phenotype Correlation in Turkish Children
43rd Annual Meeting European Society for Paediatric Endocrinology, Switzerland, pp.109, (Full Text)
- Publication Type: Conference Paper / Full Text
- Country: Switzerland
- Page Numbers: pp.109
- Istanbul University Affiliated: Yes