A gene for an autosomal dominant scleroatrophic syndrome predisposing to skin cancer (Huriez syndrome) maps to chromosome 4q23

Am J Hum Genet. 2000 Jan;66(1):326-30. doi: 10.1086/302718.
No abstract available

Publication types

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

MeSH terms

  • Abnormalities, Multiple / genetics*
  • Abnormalities, Multiple / pathology
  • Carcinoma, Squamous Cell / genetics*
  • Carcinoma, Squamous Cell / pathology
  • Chromosome Mapping
  • Chromosomes, Human, Pair 4*
  • Haplotypes
  • Humans
  • Keratoderma, Palmoplantar / congenital
  • Keratoderma, Palmoplantar / genetics*
  • Keratoderma, Palmoplantar / pathology
  • Limb Deformities, Congenital / genetics*
  • Limb Deformities, Congenital / pathology
  • Lod Score
  • Microsatellite Repeats / genetics
  • Nail Diseases / congenital
  • Nail Diseases / genetics*
  • Nail Diseases / pathology
  • Pedigree
  • Risk Factors
  • Skin Neoplasms / genetics*
  • Skin Neoplasms / pathology
  • Syndrome