2011-12-01
Associations of common variants at 1p11.2 and 14q24.1 (RAD51l1) with breast cancer risk and heterogeneity by tumor subtype: Findings from the Breast Cancer Association Consortium
Publication
Publication
Human Molecular Genetics , Volume 20 - Issue 23 p. 4693- 4706
| Additional Metadata | |
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| doi.org/10.1093/hmg/ddr368, hdl.handle.net/1765/55319 | |
| Human Molecular Genetics | |
| Organisation | Department of Clinical Genetics |
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Figueroa, J., García-Closas, M., Humphreys, M., Platte, R., Hopper, J., Southey, M., Apicella, C., Hammet, F., Schmidt, M., Broeks, A., Tollenaar, R., van 't Veer, L., Fasching, P., Beckmann, M., Ekici, A., Strick, R., Peto, J., dos Santos Silva, I., Fletcher, O., … Spurdle, A. (2011). Associations of common variants at 1p11.2 and 14q24.1 (RAD51l1) with breast cancer risk and heterogeneity by tumor subtype: Findings from the Breast Cancer Association Consortium. Human Molecular Genetics, 20(23), 4693–4706.https://doi.org/10.1093/hmg/ddr368 |
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