Reading Between the Lines: A Comparison of Responders and Non-responders to a Family History Questionnaire and Implications for Cancer Genetic Counselling
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Link
http://www.springerlink.com/index/pdf/10.1007/s10897-011-9399-0
Reference18 articles.
1. Armel, S. R., McCuaig, J., Finch, A., Demsky, R., Panzarella, T., Murphy, J., et al. (2009). The effectiveness of family history questionnaires in cancer genetic counselling. Journal of Genetic Counseling, 18, 366–378.
2. Armel, S. R., Hitchman, K., Millar, K., Zahavich, L., Demsky, R., Murphy, J., et al. (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. doi: 10.1007/s10897-011-9359-8 .
3. Cappelli, M., Surh, L., Humphreys, L., Verma, S., Loga, D., Hunter, A., et al. (1999). Psychological and social determinants of women’s decisions to undergo genetic counseling and testing for breast cancer. Clinical Genetics, 55, 419–430.
4. Culver, J., Burke, W., Yasui, Y., Durfy, S., & Press, N. (2001). Participation in breast cancer genetic counseling: the influence of educational level, ethnic background, and risk perception. Journal of Genetic Counseling, 10, 215–231.
5. Ford, M. E., Hensley Alford, S., Britton, D., McClary, B., & Gordon, H. S. (2007). Factors influencing perceptions of breast cancer genetic counseling among women in an urban health care system. Journal of Genetic Counseling, 16, 735–753.
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