1. American Medical Association. Informed consent. http://www.ama-assn.org/ama/pub/physician-resources/medical-ethics/code-medical-ethics/opinion808.page . Accessed November 8, 2013.
2. Andersen, J., Oyen, N., Bjorvatn, C., & Gjengdal, E. (2008). Living with long QT syndrome: a qualitative study of coping with increased risk of sudden cardiac death. Journal of Genetic Counseling, 17, 489–498.
3. Armstrong, K., Calzone, K., Stopfer, J., Fitzgerald, G., Coyne, J., & Weber, B. (2000). Factors associated with decisions about clinical BRCA1/2 testing. Cancer Epidemiology, Biomarkers & Prevention, 9(11), 1251–1254.
4. Auerbach, C., & Silverstein, L. (2003). Qualitative data: An introduction to coding and analysis. New York: New York University Press.
5. Balmana, J., Stoffel, E. M., Emmons, K. M., Garber, J. E., & Syngal, S. (2004). Comparison of motivations and concerns for genetic testing in hereditary colorectal and breast cancer syndromes. Journal of Medical Genetics, 41(4), e44.