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

Παρόμοια τεκμήρια

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