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

Samankaltaisia teoksia

• Milroy disease and the VEGFR-3 mutation phenotype
  Tekijä: Brice, G, et al.
  Julkaistu: (2005)
• Analysis of the phenotypic abnormalities in lymphoedema-distichiasis syndrome in 74 patients with FOXC2 mutations or linkage to 16q24
  Tekijä: Brice, G, et al.
  Julkaistu: (2002)
• Reduction of the genetic interval for lymphoedema-distichiasis to below 2 Mb
  Tekijä: BELL, R, et al.
  Julkaistu: (2000)
• A Novel Splice-Site Mutation in VEGFC Is Associated with Congenital Primary Lymphoedema of Gordon
  Tekijä: Nadarajah, Noeline, et al.
  Julkaistu: (2018)
• Mapping of primary congenital lymphedema to the 5q35.3 region.
  Tekijä: Evans, A L, et al.
  Julkaistu: (1999)