Variable phenotype and associations in chromosome 22q11.2 microdeletion

Am J Med Genet A. 2006 Mar 15;140(6):659-60. doi: 10.1002/ajmg.a.31120.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Chromosome Deletion*
  • Chromosome Disorders / genetics
  • Chromosomes, Human, Pair 22 / genetics*
  • Down Syndrome / genetics
  • Heart Defects, Congenital / genetics
  • Humans
  • Phenotype