A paternal wash in Apert syndrome

Nat Genet. 1996 May;13(1):9-10. doi: 10.1038/ng0596-9.
No abstract available

Publication types

  • Comment
  • News

MeSH terms

  • Acrocephalosyndactylia / genetics*
  • Fathers
  • Female
  • Genomic Imprinting*
  • Humans
  • Male
  • Oogenesis
  • Point Mutation
  • Receptor Protein-Tyrosine Kinases / genetics*
  • Receptor, Fibroblast Growth Factor, Type 2
  • Receptors, Fibroblast Growth Factor / genetics*
  • Spermatogenesis

Substances

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