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Results: 1-9 |
Results: 9
Sporadic multiple primary melanoma cases: CDKN2A germline mutations with afounder effect
Authors: Auroy, S Avril, MF Chompret, A Pham, D Goldstein, AM Bianchi-Scarra, G Frebourg, T Joly, P Spatz, A Rubino, C Demenais, F Bressac-de Paillerets, B
Citation: S. Auroy et al., Sporadic multiple primary melanoma cases: CDKN2A germline mutations with afounder effect, GENE CHROM, 32(3), 2001, pp. 195-202
Association between germ cell tumours, large numbers of naevi, atypical naevi and melanoma
Authors: Avril, MF Chompret, A Verne-Fourment, L Terrier-Lacombe, MJ Spatz, A Fizazi, K Bressac-de Paillerets, B Demenais, F Theodore, C
Citation: Mf. Avril et al., Association between germ cell tumours, large numbers of naevi, atypical naevi and melanoma, MELANOMA RE, 11(2), 2001, pp. 117-122
Patterns of familial aggregation of three melanoma risk factors: great number of naevi, light phototype and high degree of sun exposure
Authors: Briollais, L Chompret, A Guilloud-Bataille, M Bressac-de Paillerets, B Avril, MF Demenais, F
Citation: L. Briollais et al., Patterns of familial aggregation of three melanoma risk factors: great number of naevi, light phototype and high degree of sun exposure, INT J EPID, 29(3), 2000, pp. 408-415
Individuals with presumably hereditary uveal melanoma do not harbour germline mutations in the coding regions of either the P16(INK4A), P14(ARF) or cdk4 genes
Authors: Soufir, N Bressac-de Paillerets, B Desjardins, L Levy, C Bombled, J Gorin, I Schlienger, P Stoppa-Lyonnet, D
Citation: N. Soufir et al., Individuals with presumably hereditary uveal melanoma do not harbour germline mutations in the coding regions of either the P16(INK4A), P14(ARF) or cdk4 genes, BR J CANC, 82(4), 2000, pp. 818-822
Extensive molecular screening for hereditary non-polyposis colorectal cancer
Authors: Dieumegard, B Grandjouan, S Sabourin, JC Le Bihan, ML Lefrere, I",Bellefqih,"Pignon, JP Rougier, P Lasser, P Benard, J Couturier, D Bressac-de Paillerets, B
Citation: B. Dieumegard et al., Extensive molecular screening for hereditary non-polyposis colorectal cancer, BR J CANC, 82(4), 2000, pp. 871-880
p53 germline mutations in childhood cancers and cancer risk for carrier individuals
Authors: Chompret, A Brugieres, L Ronsin, M Gardes, M Dessarps-Freichey, F Abel, A Hua, D Ligot, L Dondon, MG Bressac-de Paillerets, B Frebourg, T Lemerle, J Bonaiti-Pellie, C Feunteun, J
Citation: A. Chompret et al., p53 germline mutations in childhood cancers and cancer risk for carrier individuals, BR J CANC, 82(12), 2000, pp. 1932-1937
A single genetic origin for the G101W CDKN2A mutation in 20 melanoma-pronefamilies
Authors: Ciotti, P Struewing, JP Mantelli, M Chompret, A Avril, MF Santi, PL Tucker, MA Bianchi-Scarra, G Bressac-de Paillerets, B Goldstein, AM
Citation: P. Ciotti et al., A single genetic origin for the G101W CDKN2A mutation in 20 melanoma-pronefamilies, AM J HU GEN, 67(2), 2000, pp. 311-319
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
hMSH2 (human homolog of MutS)
Authors: Soussi, T Frebourg, T Bressac-de Paillerets, B
Citation: T. Soussi et al., hMSH2 (human homolog of MutS), B CANCER, 85(11), 1998, pp. 921-921
Risultati: 1-9 |