GLI3 is rarely implicated in OFD syndromes with midline abnormalities

Hum Mutat. 2011 Nov;32(11):1332-3. doi: 10.1002/humu.21570. Epub 2011 Sep 19.
No abstract available

Publication types

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

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Humans
  • Kruppel-Like Transcription Factors / genetics*
  • Mutation*
  • Nerve Tissue Proteins / genetics*
  • Pallister-Hall Syndrome / pathology*
  • Polydactyly / pathology*
  • Syndactyly / pathology*

Substances

  • Kruppel-Like Transcription Factors
  • Nerve Tissue Proteins