Characterization of 10p deletions suggests two nonoverlapping regions contribute to the DiGeorge syndrome phenotype

Am J Hum Genet. 1998 Feb;62(2):495-8. doi: 10.1086/301718.
No abstract available

Publication types

  • Letter
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Chromosome Mapping
  • Chromosomes, Human, Pair 10*
  • Chromosomes, Human, Pair 22
  • DiGeorge Syndrome / genetics*
  • Female
  • Gene Deletion*
  • Genetic Markers
  • Humans
  • Male
  • Phenotype
  • Sequence Tagged Sites

Substances

  • Genetic Markers