A novel 22q11.2 microdeletion in DiGeorge syndrome

Am J Hum Genet. 1999 Feb;64(2):659-66. doi: 10.1086/302235.
No abstract available

Publication types

  • Letter

MeSH terms

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