Authors:
Tonin, PN
Mes-Masson, AM
Narod, SA
Ghadirian, P
Provencher, D
Citation: Pn. Tonin et al., Founder BRCA1 and BRCA2 mutations in French Canadian ovarian cancer cases unselected for family history, CLIN GENET, 55(5), 1999, pp. 318-324
Authors:
Wang-Gohrke, S
Weikel, W
Risch, H
Vesprini, D
Abrahamson, J
Lerman, C
Godwin, A
Moslehi, R
Olipade, O
Brunet, JS
Stickeler, E
Kieback, DG
Kreienberg, R
Weber, B
Narod, SA
Runnebaum, IB
Citation: S. Wang-gohrke et al., Intron variants of the p53 gene are associated with increased risk for ovarian cancer but not in carriers of BRCA1 or BRCA2 germline mutations, BR J CANC, 81(1), 1999, pp. 179-183
Authors:
Foulkes, WD
Brunet, JS
Warner, E
Goodwin, PJ
Meschino, W
Narod, SA
Goss, PE
Glendon, G
Citation: Wd. Foulkes et al., The importance of a family history of breast cancer in predicting the presence of a BRCA mutation, AM J HU GEN, 65(6), 1999, pp. 1776-1779
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