Cleidocranial dysplasia in a Polish population: high frequency of the R193X mutation

Clin Genet. 2006 Aug;70(2):167-9. doi: 10.1111/j.1399-0004.2006.00648.x.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Cleidocranial Dysplasia / diagnosis
  • Cleidocranial Dysplasia / genetics*
  • Core Binding Factor Alpha 1 Subunit / genetics*
  • Female
  • Humans
  • Male
  • Molecular Sequence Data
  • Mutation
  • Poland

Substances

  • Core Binding Factor Alpha 1 Subunit

Associated data

  • GENBANK/AF001443
  • GENBANK/AF001444
  • GENBANK/AF001445
  • GENBANK/AF001446
  • GENBANK/AF001447
  • GENBANK/AF001448
  • GENBANK/AF001449
  • GENBANK/AF001450
  • OMIM/119600