Microdeletion of 16p11.2 associated with endocardial fibroelastosis

Am J Med Genet A. 2010 Sep;152A(9):2383-6. doi: 10.1002/ajmg.a.33562.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Autopsy
  • Chromosomes, Human, Pair 16*
  • Endocardial Fibroelastosis / congenital
  • Endocardial Fibroelastosis / diagnosis
  • Endocardial Fibroelastosis / genetics*
  • Family
  • Fatal Outcome
  • Humans
  • Infant, Newborn
  • Male
  • Sequence Deletion*