Effect on splicing of a silent FGFR2 mutation in Crouzon syndrome

Nat Genet. 1995 Mar;9(3):232-3. doi: 10.1038/ng0395-232.
No abstract available

Publication types

  • Letter
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Base Sequence
  • Craniofacial Dysostosis / genetics*
  • DNA Primers / genetics
  • DNA, Recombinant
  • Humans
  • Molecular Sequence Data
  • Mutation
  • Receptors, Fibroblast Growth Factor / genetics*

Substances

  • DNA Primers
  • DNA, Recombinant
  • Receptors, Fibroblast Growth Factor