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Open Peer Commentaries

Participation in Research and Social Context: The Case of Population-Based Cancer Registration, Surveillance, and Research

Pages 41-42 | Published online: 17 Nov 2008

REFERENCES

  • California Health and Safety Code § 103885(g)(5),(8) (2006)
  • Clarke , C. and Glaser , S. 2007 . Declines in breast cancer after the WHI: Apparent impact of hormone therapy . Cancer Causes and Control , 18 ( 8 ) : 847 – 852 .
  • California Cancer Registry (CCR) . 2008 . Policies and procedures for access to and disclosure of confidential data from the California cancer registry ver. 04.4 (February 2008) Available at: http://www.ccrcal.org/PDF/CCRDataAccessDisclo_v04.4.pdf (accessed September 2, 2008)
  • de Melo-Martin , I. 2008 . A duty to participate in research: Does social context matter? . American Journal of Bioethics , 8 ( 10 ) : 28 – 36 .
  • Fairchild , A. , Bayer , R. and Colgrove , J. 2007 . Searching eyes: Privacy, the state, and disease surveillance in America , Berkeley, CA : University of California Press .
  • Surveillance Epidemiology and End Results (SEER) . 2008 . Surveillance epidemiology and end results program of the National Cancer Institute Available at: http://seer.cancer.gov/about/ (accessed September 2, 2008)

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