Opitz GBBB syndrome and the 22q11.2 deletion

Am J Med Genet. 1996 Mar 29;62(3):318. doi: 10.1002/(SICI)1096-8628(19960329)62:3<318::AID-AJMG21>3.0.CO;2-M.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22*
  • Humans
  • Hypertelorism / complications
  • Hypertelorism / genetics*
  • Hypospadias / complications
  • Hypospadias / genetics*
  • Infant, Newborn
  • Male