All in the Family: Barriers and Motivators to the Use of Cancer Family History Questionnaires and the Impact on Attendance Rates
Author:
Publisher
Wiley
Subject
Genetics(clinical)
Link
http://link.springer.com/content/pdf/10.1007/s10897-014-9813-5
Reference26 articles.
1. Acton, R. T., Burst, N. M., Casebeer, L., Ferguson, S. M., Greene, P., Laird, B. L., & Leviton, L. (2000). Knowledge, attitudes, and behaviors of alabama’s primary care physicians regarding cancer genetics. Academic Medicine, 75(8), 850–852.
2. Anderson, B., McLosky, J., Wasilevich, E., Lyon-Callo, S., Duquette, D., & Copeland, G. (2012). Barriers and facilitators for utilization of genetic counseling and risk assessment services in young female breast cancer survivors. Journal of Cancer Epidemiology, 2012, 298745. doi: 10.1155/2012/298745 .
3. Appleby-Tagoe, J. H., Foulkes, W. D., & Palma, L. (2012). Reading between the lines: a comparison of responders and non-responders to a family history questionnaire and implications for cancer genetic counselling. Journal of Genetic Counseling, 21(2), 273–291. doi: 10.1007/s10897-011-9399-0 .
4. Armel, S. R., McCuaig, J., Finch, A., Demsky, R., Panzarella, T., Murphy, J., & Rosen, B. (2009). The effectiveness of family history questionnaires in cancer genetic counseling. Journal of Genetic Counseling, 18(4), 366–378. doi: 10.1007/s10897-009-9228-x .
5. Armel, S. R., Hitchman, K., Millar, K., Zahavich, L., Demsky, R., Murphy, J., & Rosen, B. (2011). The use of family history questionnaires: an examination of genetic risk estimates and genetic testing eligibility in the non-responder population. Journal of Genetic Counseling, 20(4), 355–364. doi: 10.1007/s10897-011-9359-8 .
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