Deletion mapping of 22q11 in CATCH22 syndrome: identification of a second critical region

Am J Hum Genet. 1996 Jun;58(6):1377-81.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Centromere
  • Chromosome Mapping
  • Chromosomes, Human, Pair 22*
  • Congenital Abnormalities / genetics*
  • Genetic Markers
  • Humans
  • In Situ Hybridization, Fluorescence
  • Sequence Deletion*
  • Syndrome

Substances

  • Genetic Markers