Autosomal dominant "Opitz" GBBB syndrome due to a 22q11.2 deletion

Am J Med Genet. 1996 Aug 23;64(3):525-6. doi: 10.1002/ajmg.1320640304.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Chromosome Aberrations / genetics*
  • Chromosome Deletion*
  • Chromosome Disorders
  • Chromosomes, Human, Pair 22 / genetics*
  • Female
  • Genes, Dominant
  • Humans
  • Male
  • Syndrome