[Coffin-Lowry syndrome. Description of 2 cases]

Bol Med Hosp Infant Mex. 1986 Jun;43(6):378-81.
[Article in Spanish]
No abstract available

Publication types

  • Case Reports
  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Child
  • Female
  • Genetic Linkage
  • Humans
  • Intellectual Disability / genetics
  • Male
  • Orofaciodigital Syndromes / genetics*
  • Phenotype
  • Spine / abnormalities
  • X Chromosome