Adrenocortical tumor in patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency

Samankaltaisia teoksia

• Phenotype of patients with congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
  Tekijä: Dung, Vu Chi, et al.
  Julkaistu: (2015)
• Mutation spectrum of CYP21A2 and correlation between genotype – phenotype in 81 Vietnamese patients with congenital adrenal hyperplasia due to 21-hydroxylase defficiency
  Tekijä: Dung, Vu Chi, et al.
  Julkaistu: (2013)
• Congenital adrenal hyperplasia with cholestatic jaundice: a case report
  Tekijä: Mai, DoThi Thanh, et al.
  Julkaistu: (2015)
• Updated registry of congenital adrenal hyperplasia at the north pediatric referral centre of Vietnam
  Tekijä: Dung, Vu Chi, et al.
  Julkaistu: (2015)
• AB074. Registry of congenital adrenal hyperplasia at the north pediatric referral centre of Vietnam during 15 years
  Tekijä: Dung, Vu Chi, et al.
  Julkaistu: (2015)