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Results: 1-11 |
Results: 11
No germline mutations in CDKN2A (p16) in patients with squamous cell cancer of the head and neck and second primary tumours
Authors: Jefferies, S Edwards, SM Hamoudi, RA A'Hern, R Foulkes, W Goldgar, D Collaborators, MPT Eeles, R
Citation: S. Jefferies et al., No germline mutations in CDKN2A (p16) in patients with squamous cell cancer of the head and neck and second primary tumours, BR J CANC, 85(9), 2001, pp. 1383-1386
The pathology of familial breast cancer: Histological features of cancers in families not attributable to mutations in BRCA1 or BRCA2
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
Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22
Authors: Rahman, N Teare, MD Seal, S Renard, H Mangion, J Cour, C Thompson, D Shugart, Y Eccles, D Devilee, P Meijers, H Nathanson, KL Neuhausen, SL Weber, B Chang-Claude, J Easton, DF Goldgar, D Stratton, MR
Citation: N. Rahman et al., Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22, ONCOGENE, 19(36), 2000, pp. 4170-4173
Suggestive evidence for a site specific prostate cancer gene on chromosome1p36
Authors: Badzioch, M Eeles, R Leblanc, G Foulkes, WD Giles, G Edwards, S Goldgar, D Hopper, JL Bishop, DT Moller, P Heimdal, K Easton, D
Citation: M. Badzioch et al., Suggestive evidence for a site specific prostate cancer gene on chromosome1p36, J MED GENET, 37(12), 2000, pp. 947-948
The exon 13 duplication in the BRCA1 gene is a founder mutation present ingeographically diverse populations
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
Linkage analysis of 56 multiplex families excludes the Cowden disease genePTEN as a major contributor to familial breast cancer
Authors: Shugart, YY Cour, C Renard, H Lenoir, G Goldgar, D Teare, D Easton, D Rahman, N Gusterton, R Seal, S Barfoot, R Stratton, M Mangion, J Peelen, T van den Ouweland, A Meijers, H Devilee, P Eccles, D Lynch, H Weber, B Stoppa-Lyonnet, D Bignon, YJ
Citation: Yy. Shugart et al., Linkage analysis of 56 multiplex families excludes the Cowden disease genePTEN as a major contributor to familial breast cancer, J MED GENET, 36(9), 1999, pp. 720-721
Germline brca2 sequence variants in patients with ocular melanoma
Authors: Sinilnikova, OM Egan, KM Quinn, JL Boutrand, L Lenoir, GM Stoppa-Lyonnet, D Desjardins, L Levy, C Goldgar, D Gragcoudas, ES
Citation: Om. Sinilnikova et al., Germline brca2 sequence variants in patients with ocular melanoma, INT J CANC, 82(3), 1999, pp. 325-328
The role of genetic factors in predisposition to squamous cell cancer of the head and neck
Authors: Jefferies, S Eeles, R Goldgar, D A'Hern, R Henk, JM Gore, M
Citation: S. Jefferies et al., The role of genetic factors in predisposition to squamous cell cancer of the head and neck, BR J CANC, 79(5-6), 1999, pp. 865-867
An Alu-mediated 6-kb duplication in the BRCA1 gene: A new founder mutation?
Authors: Puget, N Sinilnikova, OM Stoppa-Lyonnet, D Audoynaud, C Pages, S Lynch, HT Goldgar, D Lenoir, GM Mazoyer, S
Citation: N. Puget et al., An Alu-mediated 6-kb duplication in the BRCA1 gene: A new founder mutation?, AM J HU GEN, 64(1), 1999, pp. 300-302
Genetics and epidemiology of hereditary breast cancer
Authors: Devilee, P Barkardottir, RB Bevilacqua, G Bignon, YJ Bishop, T Borg, A Borresen-Dale, AL Chang-Claude, J Easton, D Eyfjord, J Feunteun, J Goldgar, D Haites, N Holm, N Kruse, T Larsson, C Lenoir, G Lidereau, R Nevanlinna, H Ponder, B Scherneck, S Schmitt, F Sobol, H Solomon, E Spurr, N Steel, M Stratton, M Varley, J Vasen, H Vassilaros, S Wagner, T Willems, P Winqvist, R
Citation: P. Devilee et al., Genetics and epidemiology of hereditary breast cancer, BIOM HLTH R, 24, 1998, pp. 339-346
Implication of germline BRCA2 gene mutations for the occurrence of ocular melanoma and pancreatic cancer
Authors: Serova-Sinilnikova, O Egan, K Boutrand, L Stoppa-Lyonnet, D Desjardins, L Levy, C Bignon, YJ Lasset, C Haguenauer, O Goldgar, D Lenoir, GM
Citation: O. Serova-sinilnikova et al., Implication of germline BRCA2 gene mutations for the occurrence of ocular melanoma and pancreatic cancer, EUROCANCER 98, 1998, pp. 113-114
Risultati: 1-11 |