Corrigendum: The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency

Ítems similars

• The Complexities in Genotyping of Congenital Adrenal Hyperplasia: 21-Hydroxylase Deficiency
  per: Pignatelli, Duarte, et al.
  Publicat: (2019)
• Metabolic Perspectives for Non-classical Congenital Adrenal Hyperplasia With Relation to the Classical Form of the Disease
  per: Macut, Djuro, et al.
  Publicat: (2019)
• Editorial: Congenital Adrenal Hyperplasia, Unresolved Issues and Implications on Clinical Management
  per: Livadas, Sarantis, et al.
  Publicat: (2020)
• Quality of Life in Men With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
  per: Verhees, Myrthe J. M., et al.
  Publicat: (2021)
• Disease expression and molecular genotype in congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
  per: Speiser, P W, et al.
  Publicat: (1992)