Identification of eight novel VEGFR-3 mutations in families with primary congenital lymphoedema

J Med Genet. 2003 Sep;40(9):697-703. doi: 10.1136/jmg.40.9.697.
No abstract available

Publication types

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

MeSH terms

  • DNA / chemistry
  • DNA / genetics
  • DNA Mutational Analysis
  • Family Health
  • Female
  • Genotype
  • Haplotypes
  • Humans
  • Lymphedema / congenital
  • Lymphedema / genetics*
  • Male
  • Mutation
  • Mutation, Missense
  • Pedigree
  • Sequence Deletion
  • Vascular Endothelial Growth Factor Receptor-3 / genetics*

Substances

  • DNA
  • Vascular Endothelial Growth Factor Receptor-3