Author:
Randall Armel Susan,McCuaig Jeanna,Finch Amy,Demsky Rochelle,Panzarella Tony,Murphy Joan,Rosen Barry
Reference19 articles.
1. Antoniou, A., Pharoah, P. D., Narod, S., et al. (2003). Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case series unselected for family history: a combined analysis of 22 studies. American Journal of Human Genetics, 72, 1117–1130. doi: 10.1086/375033 .
2. Berry, D. A., Iversen, E. S,. Jr, Gudbjartsson, D. F., Hiller, E. H., Garber, J. E., Peshkin, B. N., et al. (2002). BRCAPRO validation, sensitivity of genetic testing of BRCA1/BRCA2, and prevalence of other breast cancer susceptibility genes. Journal of Clinical Oncology, 20(11), 2701–2712. doi: 10.1200/JCO.2002.05.121 .
3. The Breast Cancer Linkage Consortium. (1999). Cancer risks in BRCA2 mutation carriers. Journal of the National Cancer Institute, 91(15), 1310–1316. doi: 10.1093/jnci/91.15.1310 .
4. Brener, D., Schulz, C., Schluger, A., & Offit, K. (1996). A self-administered family history questionnaire (FHQ) utilized in an outpatient setting to assess cancer risk. American Journal of Human Genetics, 59, A333.
5. Chalmers, K. I., Luker, K. A., Leinster, S. J., Ellis, I., & Booth, K. (2001). Information and support needs of women with primary relatives with breast cancer: development of the information and support needs questionnaire. Journal of Advanced Nursing, 35(4), 497–507. doi: 10.1046/j.1365-2648.2001.01866.x .
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