TBX22 mutations are a frequent cause of cleft palate

J Med Genet. 2004 Jan;41(1):68-74. doi: 10.1136/jmg.2003.010868.
No abstract available

Publication types

  • Letter
  • Multicenter Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Amino Acid Sequence / genetics
  • Chromosomes, Human, X / genetics
  • Cleft Palate / genetics*
  • Cohort Studies
  • Female
  • Genetic Diseases, X-Linked / genetics
  • Humans
  • Male
  • Molecular Sequence Data
  • Mutation / genetics*
  • Pedigree
  • T-Box Domain Proteins / chemistry
  • T-Box Domain Proteins / genetics*

Substances

  • T-Box Domain Proteins
  • TBX22 protein, human