Journal of Law, Medicine and Ethics 43 (3):464-475 (2015)

Authors
Susan Wolf
University of North Carolina, Chapel Hill
Abstract
Data are lacking with regard to participants' perspectives on return of genetic research results to relatives, including after the participant's death. This paper reports descriptive results from 3,630 survey respondents: 464 participants in a pancreatic cancer biobank, 1,439 family registry participants, and 1,727 healthy individuals. Our findings indicate that most participants would feel obligated to share their results with blood relatives while alive and would want results to be shared with relatives after their death
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DOI 10.1111/jlme.12289
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