1. Beauchamp, T., & Childress, J. (2001). Principles of biomedical ethics (5th ed.). New York: Oxford University Press.
2. Blandy, C., Chabal, F., Stoppa-Lyonnet, D., & Julian-Reynier, C. (2003). Testing participation in BRCA1/2-positive families: Initiator role of index cases. Genetic Testing, 7, 225–233. doi: 10.1089/109065703322537241 .
3. Bottorff, J. L., McCullum, M., Balneaves, L. G., Esplen, M. J., Carroll, J., Kelly, M., et al. (2005). Establishing roles in genetic nursing: Interviews with Canadian nurses. Canadian Journal of Nursing Research, 37, 96–115.
4. Buiting, K., Farber, C., Kroisel, P., Wagner, K., Brueton, L., Robertson, M. E., et al. (2000). Imprinting centre deletions in two PWS families: Implications for diagnostic testing and genetic counseling. Clinical Genetics, 58, 284–290. doi: 10.1034/j.1399-0004.2000.580406.x .
5. Burns, N., & Grove, S. K. (2001). The practice of nursing research. Conduct, critique, & utilization (5th ed.). Missouri, USA: Elsevier Sounders.