A familial syndrome of mental retardation in association with multiple congenital anomalies resembling the syndrome of Smith-Lemli-Opitz

Maandschr Kindergeneeskd. 1967 May;35(2):37-48.
No abstract available

MeSH terms

  • Congenital Abnormalities / genetics*
  • Dermatoglyphics
  • Female
  • Humans
  • Infant
  • Intellectual Disability / genetics*
  • Male