Clinical and genetic variability of oculodentodigital dysplasia

Clin Genet. 2006 Jul;70(1):71-2. doi: 10.1111/j.1399-0004.2006.00631.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Adolescent
  • Child
  • Child, Preschool
  • Connexin 43 / genetics
  • Eye Abnormalities / genetics*
  • Female
  • Fingers / abnormalities
  • Gap Junctions / genetics
  • Genes, Dominant
  • Humans
  • Middle Aged
  • Mutation
  • Phenotype
  • Syndactyly / genetics*
  • Toes / abnormalities
  • Tooth Abnormalities / genetics*

Substances

  • Connexin 43
  • GJA1 protein, human

Associated data

  • OMIM/164200