The incidence of a deletion in chromosome 22Q11 in sporadic and familial conotruncal heart disease

Eur J Pediatr. 1996 Aug;155(8):721. doi: 10.1007/BF01957162.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22*
  • Female
  • Heart Defects, Congenital / epidemiology*
  • Heart Defects, Congenital / genetics*
  • Humans
  • Incidence
  • Male
  • Prospective Studies