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2.

The role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testing
by Pharoah, Paul D P

Clinical cancer research : an official journal of the American Association for Cancer Research, 01 June 2011, Vol.17(11), pp.3742-50

13.

COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration
by Southey, Melissa C

Southey, M. C., D. J. Park, T. Nguyen-Dumont, I. Campbell, E. Thompson, A. H. Trainer, G. Chenevix-Trench, et al. 2013. “COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration.” Breast Cancer Research : BCR 15 (3): 402. doi:10.1186/bcr3434. http://dx.doi.org/10.1186/bcr3434.

15.

Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk
by Gaudet, Mia M.

Gaudet, Mia M., Karoline B. Kuchenbaecker, Joseph Vijai, Robert J. Klein, Tomas Kirchhoff, Lesley McGuffog, Daniel Barrowdale, et al. 2013. Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk. PLoS Genetics 9(3): e1003173.

17.

Common Variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 Are Associated with Breast Cancer Risk for BRCA1 and/or BRCA2 Mutation Carriers
by Antoniou, Antonis C

Antoniou, Antonis C., Karoline B. Kuchenbaecker, Penny Soucy, Jonathan Beesley, Xiaoqing Chen, Lesley McGuffog, Andrew Lee, et al. 2012. Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers. Breast Cancer Research 14(1): R33.

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