A gene for premature ovarian failure associated with eyelid malformation maps to chromosome 3q22-q23

Am J Hum Genet. 1996 May;58(5):1089-92.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Chromosome Mapping
  • Chromosomes, Human, Pair 3*
  • Eyelids / abnormalities*
  • Female
  • Humans
  • Pedigree
  • Primary Ovarian Insufficiency / genetics*
  • Primary Ovarian Insufficiency / physiopathology