A novel fibroblast growth factor receptor 2 (FGFR2) mutation associated with a mild Crouzon syndrome

Arch Ital Biol. 2011 Sep;149(3):313-7. doi: 10.4449/aib.v149i3.1379.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Craniofacial Dysostosis / genetics*
  • DNA Mutational Analysis
  • Humans
  • Imaging, Three-Dimensional
  • Magnetic Resonance Imaging
  • Male
  • Mutation / genetics*
  • Personality Inventory
  • Receptor, Fibroblast Growth Factor, Type 2 / genetics*

Substances

  • FGFR2 protein, human
  • Receptor, Fibroblast Growth Factor, Type 2