True hermaphroditism with 46,XY karyotype and a point mutation in the SRY gene

J Pediatr. 1995 Jun;126(6):1022. doi: 10.1016/s0022-3476(95)70247-4.
No abstract available

Publication types

  • Case Reports
  • Comment
  • Letter

MeSH terms

  • Disorders of Sex Development / genetics*
  • Female
  • Humans
  • Karyotyping
  • Point Mutation*
  • Sex Chromosomes