Participation in research and social context: the case of population-based cancer registration, surveillance, and research

Am J Bioeth. 2008 Oct;8(10):41-2. doi: 10.1080/15265160802478446.
No abstract available

Publication types

  • Comment

MeSH terms

  • Biomedical Research / ethics
  • Breast Neoplasms / chemically induced
  • Breast Neoplasms / epidemiology
  • California
  • Estrogen Replacement Therapy / adverse effects
  • Estrogen Replacement Therapy / statistics & numerical data
  • Female
  • Humans
  • Moral Obligations*
  • Neoplasms* / epidemiology
  • Population Surveillance*
  • Registries*
  • Research Subjects
  • SEER Program
  • Social Environment*
  • United States / epidemiology