p450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia

Documenti analoghi

• P450XXI (steroid 21-hydroxylase) gene deletions are not found in family studies of congenital adrenal hyperplasia.
  di: Matteson, K J, et al.
  Pubblicazione: (1987)
• Deletion of the steroid 21-hydroxylase and complement C4 genes in congenital adrenal hyperplasia.
  di: Rumsby, G, et al.
  Pubblicazione: (1986)
• Gene conversion-like events cause steroid 21-hydroxylase deficiency in congenital adrenal hyperplasia.
  di: Harada, F, et al.
  Pubblicazione: (1987)
• CORRIGENDUM FOR “Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society* Clinical Practice Guideline”
  Pubblicazione: (2018)
• Molecular characterization of the HLA-linked steroid 21-hydroxylase B gene from an individual with congenital adrenal hyperplasia.
  di: Rodrigues, N R, et al.
  Pubblicazione: (1987)