Smith-Lemli-Opitz syndrome in an inbred family

Am J Dis Child. 1972 Sep;124(3):431-3. doi: 10.1001/archpedi.1972.02110150129021.
No abstract available

MeSH terms

  • Abnormalities, Multiple*
  • Adult
  • Consanguinity
  • Female
  • Growth Disorders*
  • Humans
  • Infant
  • Intellectual Disability*
  • Male
  • Microcephaly*
  • Syndrome