The 17 alpha-hydroxylase deficiency found in genotypically female and male siblings, both phenotypically female

Jinrui Idengaku Zasshi. 1977 Mar;21(4):247-56.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adolescent
  • Adult
  • Amenorrhea / genetics
  • Disorders of Sex Development / genetics*
  • Female
  • Genotype
  • Humans
  • Phenotype
  • Sex Chromosomes*
  • Steroid Hydroxylases / deficiency*

Substances

  • Steroid Hydroxylases