Opitz G/BBB syndrome: clinical comparisons of families linked to Xp22 and 22q, and a review of the literature

Am J Med Genet. 1996 Mar 29;62(3):305-17. doi: 10.1002/(SICI)1096-8628(19960329)62:3<305::AID-AJMG20>3.0.CO;2-N.
No abstract available

Publication types

  • Comparative Study

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosomes, Human, Pair 22*
  • Female
  • Humans
  • Hypertelorism / complications
  • Hypertelorism / genetics*
  • Hypospadias / complications
  • Hypospadias / genetics*
  • Male
  • Pedigree
  • X Chromosome*