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Results:
1-9
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Results: 9
Authors:
Satagopan, JM
Offit, K
Foulkes, W
Robson, ME
Wacholder, S
Eng, CM
Karp, SE
Begg, CB
Citation: Jm. Satagopan et al., The lifetime risks of breast cancer in Ashkenazi Jewish carriers of BRCA1 and BRCA2 mutations, CANC EPID B, 10(5), 2001, pp. 467-473
Authors:
Rabelo, R
Foulkes, W
Gordon, PH
Wong, N
Yuan, ZQ
MacNamara, E
Chong, G
Pinsky, L
Lasko, D
Citation: R. Rabelo et al., Role of molecular diagnostic testing in familial adenomatous polyposis andhereditary nonpolyposis colorectal cancer families, DIS COL REC, 44(3), 2001, pp. 437-446
Authors:
Wong, N
Lasko, D
Rabelo, R
Pinsky, L
Gordon, PH
Foulkes, W
Citation: N. Wong et al., Genetic counseling and interpretation of genetic tests in familial adenomatous polyposis and hereditary nonpolyposis colorectal cancer, DIS COL REC, 44(2), 2001, pp. 271-279
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
Authors:
Julian-Reynier, C
Eisinger, F
Evans, G
Foulkes, W
Sobol, H
Citation: C. Julian-reynier et al., Variation in prophylactic surgery decisions, LANCET, 356(9242), 2000, pp. 1687-1687
Authors:
Rapley, EA
Barfoot, R
Bonaiti-Pellie, C
Chompret, A
Foulkes, W
Perusinghe, N
Reeve, A
Royer-Pokora, B
Schumacher, V
Shelling, A
Skeen, J
de Tourreil, S
Weirich, A
Pritchard-Jones, K
Stratton, MR
Rahman, N
Citation: Ea. Rapley et al., Evidence for susceptibility genes to familial Wilms tumour in addition to WT1, FWT1 and FWT2, BR J CANC, 83(2), 2000, pp. 177-183
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:
Foulkes, W
Shelling, AN
Citation: W. Foulkes et An. Shelling, Molecular genetics of ovarian cancer - A technical overview, METH MOL M, 39, 2000, pp. 273-290
Authors:
Warner, E
Foulkes, W
Goodwin, P
Meschino, W
Blondal, J
Paterson, C
Ozcelik, H
Goss, P
Allingham-Hawkins, D
Hamel, N
Di Prospero, L
Contiga, V
Serruya, C
Klein, M
Moslehi, R
Honeyford, J
Liede, A
Glendon, C
Brunet, JS
Narod, S
Citation: E. Warner et al., Prevalence and penetrance of BRCA1 and BRCA2 gene mutations in unselected Ashkenazi Jewish women with breast cancer, J NAT CANC, 91(14), 1999, pp. 1241-1247
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