Smith-Lemli-Opitz syndrome, cardiac defects, and spleen anomalies

Eur J Med Genet. 2013 Feb;56(2):123. doi: 10.1016/j.ejmg.2012.09.008. Epub 2012 Sep 27.
No abstract available

Publication types

  • Letter
  • Comment

MeSH terms

  • Female
  • Fetus / pathology*
  • Humans
  • Male
  • Phenotype*
  • Smith-Lemli-Opitz Syndrome / pathology*