Genetic Counseling and the Ethical Issues Around Direct to Consumer Genetic Testing
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Link
http://www.springerlink.com/index/pdf/10.1007/s10897-012-9488-8
Reference47 articles.
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2. Angrist, M. (2009). We are the genes we’ve been waiting for: rational responses to the gathering storm of personal genomics. The American Journal of Bioethics, 9(6), 30–31.
3. Armstrong, K., Micco, E., Carney, A., Stopfer, J., & Putt, M. (2005). Racial differences in the use of BRCA1/2 testing among women with a family history of breast or ovarian cancer. JAMA: The Journal of the American Medical Association, 293(14), 1729–1736.
4. Beauchamp, T., & Childress, J. (2009). Principles of biomedical ethics. USA: Oxford University Press.
5. Bloss, C., Ornowski, L., Silver, E., Cargill, M., Vanier, V., Schork, N., et al. (2010). Consumer perceptions of direct to consumer personalized genomic risk assessments. Genetics in Medicine, 12(9), 556–566.
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