Low frequency of hMSH2 mutations in Swedish HNPCC families

Int J Cancer. 1997 Feb 20;74(1):134-7. doi: 10.1002/(sici)1097-0215(19970220)74:1<134::aid-ijc22>3.0.co;2-e.
No abstract available

Publication types

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

MeSH terms

  • Colorectal Neoplasms, Hereditary Nonpolyposis / epidemiology
  • Colorectal Neoplasms, Hereditary Nonpolyposis / genetics*
  • DNA Primers
  • DNA-Binding Proteins / genetics
  • Electrophoresis, Polyacrylamide Gel
  • Family
  • Gene Frequency
  • Genetic Linkage
  • Genetic Markers
  • Humans
  • Microsatellite Repeats
  • MutS Homolog 2 Protein
  • Mutation*
  • Point Mutation
  • Polymerase Chain Reaction / methods
  • Polymorphism, Genetic*
  • Proto-Oncogene Proteins / genetics*
  • Risk Factors
  • Sweden

Substances

  • DNA Primers
  • DNA-Binding Proteins
  • Genetic Markers
  • Proto-Oncogene Proteins
  • MSH2 protein, human
  • MutS Homolog 2 Protein