Familial deletions of chromosome 22q11

Am J Med Genet. 1997 Nov 28;73(1):95-6.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Adult
  • Child
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22*
  • DiGeorge Syndrome / genetics
  • Female
  • Humans
  • Intellectual Disability / genetics
  • Male
  • Velopharyngeal Insufficiency / genetics