Participation in the Cooperative Family Registry for Breast Cancer Studies: Issues of Informed Consent-Reference-Cited by-同舟云学术

Participation in the Cooperative Family Registry for Breast Cancer Studies: Issues of Informed Consent

Published:2000-03-15 Issue:6 Volume:92 Page:452-456
ISSN:0027-8874
Container-title:JNCI: Journal of the National Cancer Institute
language:en
Short-container-title:

Author:

Daly Mary B.,Offit Kenneth,Li Frederick,Glendon Gord,Yaker Alice,West Dee,Koenig Barbara,McCredie Margaret,Venne Vicki,Nayfield Susan,Seminara Daniela

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

Link

http://academic.oup.com/jnci/article-pdf/92/6/452/9996282/452.pdf

Reference14 articles.

1. Daugherty CK. Impact of therapeutic research on informed consent and the ethics of clinical trials: a medial oncology perspective. J Clin Oncol 1999;17:1601-17.

2. Reilly P. Rethinking risks to human subjects in genetic research. Am J Hum Genet 1998;63:682-5.

3. Byers PH, Ashkenas J. Pedigrees—publish? Or perish the thought? Am J Hum Genet 1998;63:678-81.

4. Office for Protection from Research Risks, U.S. Department of Health and Human Services (DHHS). Protecting human research subjects: institutional review board guidebook. Washington (DC): DHHS; 1993.

5. Code of Federal Regulations: 45 CFR §§46.101-409 (1995).

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