The value of information and the ethics of personal-genomic screening

Am J Bioeth. 2009 Apr;9(4):26-7. doi: 10.1080/15265160802716878.
No abstract available

Publication types

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

MeSH terms

  • Evidence-Based Medicine
  • Genetic Testing / economics
  • Genetic Testing / ethics*
  • Genome, Human*
  • Health Services Accessibility / economics
  • Health Services Accessibility / ethics*
  • Humans
  • Mass Screening / economics
  • Mass Screening / ethics*
  • Mass Screening / methods
  • Mass Screening / statistics & numerical data
  • Practice Guidelines as Topic
  • Reproducibility of Results
  • United States