A Crouzon syndrome synonymous mutation activates a 5' splice site within the IIIc exon of the FGFR2 gene

Genomics. 1995 Jun 10;27(3):558-9. doi: 10.1006/geno.1995.1095.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cattle
  • Craniofacial Dysostosis / genetics*
  • Craniofacial Dysostosis / metabolism
  • DNA / genetics
  • DNA Primers / genetics
  • Exons
  • Humans
  • Molecular Sequence Data
  • Point Mutation*
  • Polymerase Chain Reaction
  • RNA Splicing / genetics*
  • Receptor Protein-Tyrosine Kinases / genetics*
  • Receptor, Fibroblast Growth Factor, Type 2
  • Receptors, Fibroblast Growth Factor / genetics*

Substances

  • DNA Primers
  • Receptors, Fibroblast Growth Factor
  • DNA
  • FGFR2 protein, human
  • Receptor Protein-Tyrosine Kinases
  • Receptor, Fibroblast Growth Factor, Type 2