Sacral appendage in a child with an FGFR2 mutation: a report and review

Am J Med Genet A. 2008 Aug 15;146A(16):2172-5. doi: 10.1002/ajmg.a.32436.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Craniofacial Dysostosis / genetics*
  • Craniosynostoses / genetics*
  • Humans
  • Infant
  • Male
  • Mutation
  • Receptor, Fibroblast Growth Factor, Type 2 / genetics*
  • Sacrum / abnormalities*
  • Tomography, X-Ray Computed

Substances

  • Receptor, Fibroblast Growth Factor, Type 2