An Overview of Molecular Diagnosis of Steroid 21-Hydroxylase Deficiency

Ítems similars

• Prenatal Diagnosis and Treatment of Steroid 21-Hydroxylase Deficiency
  per: Tajima, Toshihiro, et al.
  Publicat: (2008)
• Haplotypes of the steroid 21-hydroxylase gene region encoding mild steroid 21-hydroxylase deficiency.
  per: Haglund-Stengler, B, et al.
  Publicat: (1991)
• Profiles of 21-Carbon Steroids in 21-hydroxylase Deficiency
  per: Turcu, Adina F., et al.
  Publicat: (2015)
• Pitfalls in molecular diagnosis of 21-hydroxylase deficiency in congenital adrenal hyperplasia
  per: Kolahdouz, Mahsa, et al.
  Publicat: (2015)
• High frequency of nonclassical steroid 21-hydroxylase deficiency.
  per: Speiser, P W, et al.
  Publicat: (1985)