Clinical utility gene card for: Axenfeld-Rieger syndrome

Eur J Hum Genet. 2011 Mar;19(3). doi: 10.1038/ejhg.2010.163. Epub 2010 Oct 13.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anterior Eye Segment / abnormalities
  • Eye Abnormalities* / diagnosis
  • Eye Abnormalities* / genetics
  • Eye Diseases, Hereditary
  • Forkhead Transcription Factors / genetics
  • Genetic Testing
  • Homeobox Protein PITX2
  • Homeodomain Proteins / genetics
  • Humans
  • Prenatal Diagnosis
  • Risk Assessment
  • Sensitivity and Specificity
  • Transcription Factors / genetics

Substances

  • FOXC1 protein, human
  • Forkhead Transcription Factors
  • Homeodomain Proteins
  • Transcription Factors

Supplementary concepts

  • Axenfeld-Rieger syndrome