Chromosome 22q11 monosomy and the genetic basis of congenital heart disease

J Pediatr. 1996 Jul;129(1):1-3. doi: 10.1016/s0022-3476(96)70181-6.
No abstract available

Publication types

  • Comment
  • Editorial

MeSH terms

  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22 / genetics*
  • Heart Defects, Congenital / genetics*
  • Humans
  • Terminology as Topic