Anzahl der Einträge: 2.
Artikel
Spurdle, A. B.,
Whiley, P. J.,
Thompson, B.,
Feng, B.,
Healey, S.,
Brown, M. A.,
Pettigrew, C.,
kConFab, .,
Van Asperen, C. J.,
Weber, Bernhard H. F. ,
Dutch Belgium UV Consortium, .,
German Consortium of Hereditary Breast and Ovarian Cancer, .,
French COVAR group collaborators, . und
on behalf of the ENIGMA Consortium, .
(2012)
BRCA1 R1699Q variant displaying ambiguous functional abrogation confers intermediate breast and ovarian cancer risk.
Journal of Medical Genetics 49 (8), S. 525-532.
Goldgar, D. E.,
Healey, S.,
Dowty, J. G.,
Da Silva, L.,
Chen, X.,
Spurdle, A. B.,
Terry, M. B.,
Daly, M. J.,
Buys, S. M.,
Southey, M. C.,
Andrulis, I.,
John, E. M.,
Khanna, K. K.,
Hopper, J. L.,
Oefner, Peter J.,
Lakhani, S. und
Chenevix-Trench, G.
(2011)
Rare variants in the ATM gene and risk of breast cancer.
Breast Cancer Research 13 (4), R73.
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