CYP21 Gene Mutations in Congenital Adrenal Hyperplasia due To 21-Hydroxylase Deficiency: Genotype-Phenotype Correlation in Turkish Children

ATALAR F., WOLLNIK B., DARENDELILER F., BAŞ F., GÜNÖZ H., KAYSERILI H., ...More

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