Response to Dominguez-Valentin M et al. 2019: Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database: Genetics in Medicine

Research output: Contribution to journalArticlepeer-review

Original languageEnglish
Pages (from-to)811-812
Number of pages2
JournalGen. Med.
Volume22
Issue number4
DOIs
Publication statusPublished - 2020

Keywords

  • DNA mismatch repair protein MSH2
  • MutL protein homolog 1
  • age
  • breast cancer
  • cancer diagnosis
  • cancer registry
  • cancer risk
  • cancer screening
  • clinical practice
  • gender
  • genetic analysis
  • genetic association
  • genetic variability
  • hereditary nonpolyposis colorectal cancer
  • heterozygote
  • human
  • Letter
  • mismatch repair
  • MSH2 gene
  • patient coding
  • practice guideline
  • prospective study
  • risk assessment
  • genetics
  • information processing
  • Colorectal Neoplasms, Hereditary Nonpolyposis
  • Data Management
  • DNA Mismatch Repair
  • Humans
  • MutL Protein Homolog 1
  • Prospective Studies

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