[Holt syndrome: an autosomal dominant, heterogeneous, acral malformation]

Bol Med Hosp Infant Mex. 1982 Feb;39(2):131-3.
[Article in Spanish]
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Chromosome Aberrations / genetics
  • Chromosome Disorders
  • Female
  • Genes, Dominant
  • Humans
  • Infant, Newborn
  • Metacarpus / abnormalities*
  • Syndrome
  • Toes / abnormalities*