Additional EFNB1 mutations in craniofrontonasal syndrome

Am J Med Genet A. 2008 Aug 1;146A(15):2008-12. doi: 10.1002/ajmg.a.32388.
No abstract available

MeSH terms

  • Chromosomes, Human, X*
  • Craniosynostoses / genetics*
  • DNA / genetics
  • Ephrin-B1 / genetics*
  • Female
  • Humans
  • Male
  • Mutation*
  • Polymerase Chain Reaction
  • Sequence Analysis, DNA
  • Syndrome

Substances

  • EFNB1 protein, human
  • Ephrin-B1
  • DNA