XK aprosencephaly may be a new mutation or a dominant genetic defect

Am J Med Genet. 1989 Oct;34(2):250-1. doi: 10.1002/ajmg.1320340224.
No abstract available

Publication types

  • Letter

MeSH terms

  • Brain / abnormalities*
  • Facial Bones / abnormalities*
  • Genes, Dominant*
  • Humans
  • Mutation*
  • Syndrome