Detection of an atypical 22q11 deletion that has no overlap with the DiGeorge syndrome critical region

Am J Hum Genet. 1997 Jun;60(6):1544-8. doi: 10.1016/S0002-9297(07)64250-5.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Deletion*
  • Chromosome Mapping
  • Chromosomes, Human, Pair 22*
  • DiGeorge Syndrome / genetics*
  • Female
  • Genetic Markers
  • Humans
  • In Situ Hybridization, Fluorescence
  • Karyotyping
  • Male
  • Pedigree

Substances

  • Genetic Markers