FGFR2 mutations in Pfeiffer syndrome

Nat Genet. 1995 Feb;9(2):108. doi: 10.1038/ng0295-108.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Acrocephalosyndactylia / genetics*
  • Base Sequence
  • Female
  • Humans
  • Male
  • Molecular Sequence Data
  • Mutation*
  • Receptors, Fibroblast Growth Factor / genetics*

Substances

  • Receptors, Fibroblast Growth Factor