Choosing not to undergo predictive genetic testing for hereditary colorectal cancer syndromes: expanding our understanding of decliners and declining
Author:
Funder
National Cancer Institute
Victorian Cancer Agency
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,General Psychology
Link
http://link.springer.com/article/10.1007/s10865-016-9820-0/fulltext.html
Reference47 articles.
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2. Arribas-Ayllon, M., Sarangi, S., & Clarke, A. J. (2013). Genetic testing: Accounts of autonomy, responsibility and blame. London: Routledge.
3. Bellcross, C. A., Bedrosian, S. R., Daniels, E., Duquette, D., Hampel, H., Jasperson, K., et al. (2012). Implementing screening for Lynch syndrome among patients with newly diagnosed colorectal cancer: Summary of a public health/clinical collaborative meeting. Genetics in Medicine, 14, 152–162.
4. Breheny, N., Geelhoed, E., Goldblatt, J., Ee, H., & O’Leary, P. (2006). Economic evaluation of the familial cancer programme in Western Australia: predictive genetic testing for familial adenomatous polyposis and hereditary non-polyposis colorectal carcinoma. PublicHealth Genomics, 9, 98–106.
5. Bunton, R., & Petersen, A. (2005). Genetic Governance: Health. London: Risk and Ethics in a Biotech Era.
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