An apparently nonsyndromic infant with the association of anorectal and cardiovascular anomalies and a 22q11 deletion

Am J Med Genet. 2002 Sep 15;112(1):114-5. doi: 10.1002/ajmg.10620.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Anal Canal / abnormalities*
  • Chromosome Deletion*
  • Chromosomes, Human, Pair 22*
  • Female
  • Heart Defects, Congenital / diagnosis*
  • Humans
  • Infant, Newborn
  • Rectum / abnormalities*