Pfeiffer syndrome is not caused by haploinsufficient mutations of FGFR2

J Craniofac Genet Dev Biol. 2000 Apr-Jun;20(2):109-12.
No abstract available

Publication types

  • Comment
  • Letter

MeSH terms

  • Exons
  • Foot Deformities / genetics
  • Hand Deformities / genetics
  • Humans
  • Mutation*
  • Polydactyly / genetics
  • Receptor Protein-Tyrosine Kinases / genetics*
  • Receptor, Fibroblast Growth Factor, Type 2
  • Receptors, Fibroblast Growth Factor / genetics*
  • Syndrome

Substances

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