Low frequency of inherited deletions of 22q11

Am J Med Genet. 1999 Aug 27;85(5):513-4. doi: 10.1002/(sici)1096-8628(19990827)85:5<513::aid-ajmg16>3.0.co;2-j.
No abstract available

Publication types

  • Letter

MeSH terms

  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22*
  • DiGeorge Syndrome / genetics
  • Female
  • Genetic Diseases, Inborn / genetics*
  • Genetic Markers
  • Heart Defects, Congenital / genetics
  • Humans
  • In Situ Hybridization, Fluorescence
  • Male
  • Syndrome
  • Velopharyngeal Insufficiency / genetics

Substances

  • Genetic Markers