Results: 1-6 |
Results: 6

Authors: Tavtigian, SV Simard, J Teng, DHF Abtin, V Baumgard, M Beck, A Camp, NJ Carillo, AR Chen, Y Dayananth, P Desrochers, M Dumont, M Farnham, JM Frank, D Frye, C Ghaffari, S Gupte, JS Hu, R Iliev, D Janecki, T Kort, EN Laity, KE Leavitt, A Leblanc, G McArthur-Morrison, J Pederson, A Penn, B Peterson, KT Reid, JE Richards, S Schroeder, M Smith, R Snyder, SC Swedlund, B Swensen, J Thomas, A Tranchant, M Woodland, AM Labrie, F Skolnick, MH Neuhausen, S Rommens, J Cannon-Albright, LA
Citation: Sv. Tavtigian et al., A candidate prostate cancer susceptibility gene at chromosome 17p, NAT GENET, 27(2), 2001, pp. 172-180

Authors: Slattery, ML Yakumo, K Hoffman, M Neuhausen, S
Citation: Ml. Slattery et al., Variants of the VDR gene and risk of colon cancer (United States), CANC CAUSE, 12(4), 2001, pp. 359-364

Authors: Lakhani, SR Gusterson, BA Jacquemier, J Sloane, JP Anderson, TJ van de Vijver, MJ Venter, D Freeman, A Antoniou, A McGuffog, L Smyth, E Steel, CM Haites, N Scott, RJ Goldgar, D Neuhausen, S Daly, PA Ormiston, W McManus, R Scherneck, S Ponder, BAJ Futreal, PA Peto, J Stoppa-Lyonnet, D Bignon, YJ Struewing, JP Bishop, DT Klijn, JGM Devilee, P Cornelisse, CJ Lasset, C Lenoir, G Barkardottir, RB Egilsson, V Hamann, U Chang-Claude, J Sobol, H Weber, B Easton, DF Stratton, MR
Citation: Sr. Lakhani et al., The pathology of familial breast cancer: Histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2, CLIN CANC R, 6(3), 2000, pp. 782-789

Authors: Lewis, C Book, L Black, J Sawitzke, A Cannon-Albright, L Zone, J Neuhausen, S
Citation: C. Lewis et al., Celiac disease and human leukocyte antigen genotype: Accuracy of diagnosisin self-diagnosed individuals, dosage effect, and sibling risk, J PED GASTR, 31(1), 2000, pp. 22-27

Authors: Mazoyer, S Leary, J Kirk, J Fleischmann, E Wagner, T Claes, K Messiaen, L Foulkes, W Desrochers, M Simard, J Phelan, CM Kwan, E Narod, SA Vahteristo, P Nevanlinna, H Durando, X Bignon, YJ Peyrat, JP Bonnardel, C Sinilnikova, OM Puget, N Lenoir, GM Mazoyer, S Audoynaud, C Goldgar, D Maugard, C Caux, V Gad, S Stoppa-Lyonnet, D Nogues, C Lidereau, R Machavoine, C Bressac-de Paillerets, B Kuschel, B Betz, B Niederacher, D Beckmann, MW Hamann, U Gayther, SA Ponder, BAP Robinson, M Taylor, GR Bishop, T Catteau, A Solomon, E Cohen, B Steel, M Collins, N Stratton, M van der Looij, M Olah, E Miller, NJ Barton, DE Sverdlov, RS Friedman, E Radice, P Montagna, M Sensi, E Caligo, M van Eijk, R Devilee, P van der Luijt, R Heimdal, K Moller, P Borg, A Diez, O Cortes, J Domenech, M Baiget, M Osorio, A Benitez, J Borg, A Maillet, P Sappino, AP Ozdag, H Ozcelik, T Ozturk, M Rohlfs, EM Boyd, J McDermott, D Offit, K Unger, M Nathanson, K Weber, BL Sellers, TA Hampton, E Couch, FJ Neuhausen, S
Citation: S. Mazoyer et al., The exon 13 duplication in the BRCA1 gene is a founder mutation present ingeographically diverse populations, AM J HU GEN, 67(1), 2000, pp. 207-212

Authors: Rebbeck, TR Kantoff, PN Krithivas, K Neuhausen, S Blackwood, MA Godwin, AK Daly, MB Narod, SA Garber, JE Lynch, HT Weber, BL Brown, M
Citation: Tr. Rebbeck et al., Modification of BRCA1-associated breast cancer risk by the polymorphic androgen-receptor CAG repeat, AM J HU GEN, 64(5), 1999, pp. 1371-1377
Risultati: 1-6 |