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Results: 1-9 |
Results: 9
Haplotype analysis in Icelandic and Finnish BRCA2 999del5 breast cancer families
Authors: Barkardottir, RB Sarantaus, L Arason, A Vehmanen, P Bendahl, PO Kainu, T Syrjakoski, K Krahe, R Huusko, P Pyrhonen, S Holli, K Kallioniemi, OP Egilsson, V Kere, J Nevanlinna, H
Citation: Rb. Barkardottir et al., Haplotype analysis in Icelandic and Finnish BRCA2 999del5 breast cancer families, EUR J HUM G, 9(10), 2001, pp. 773-779
BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age
Authors: Bergthorsson, JT Ejlertsen, B Olsen, JH Borg, A Nielsen, KV Barkardottir, RB Klausen, S Mouridsen, HT Winther, K Fenger, K Niebuhr, A Harboe, TL Niebuhr, E
Citation: Jt. Bergthorsson et al., BRCA1 and BRCA2 mutation status and cancer family history of Danish women affected with multifocal or bilateral breast cancer at a young age, J MED GENET, 38(6), 2001, pp. 361-368
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
Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus
Authors: Kainu, T Juo, SHH Desper, R Schaffer, AA Gillanders, E Rozenblum, E Freas-Lutz, D Weaver, D Stephan, D Bailey-Wilson, J Kallioniemi, OP Tirkkonen, M Syrjakoski, K Kuukasjarvi, T Koivisto, P Karhu, R Holli, K Arason, A Johannesdottir, G Bergthorsson, JT Johannsdottir, H Egilsson, V Barkardottir, RB Johannsson, O Haraldsson, K Sandberg, T Holmberg, E Gronberg, H Olsson, H Borg, A Vehmanen, P Eerola, H Heikkila, P Pyrhonen, S Nevanlinna, H
Citation: T. Kainu et al., Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus, P NAS US, 97(17), 2000, pp. 9603-9608
Chromosome 8p alterations in sporadic and BRCA2 999del5 linked breast cancer
Authors: Sigbjornsdottir, BI Ragnarsson, G Agnarsson, BA Chen, HP Barkardottir, RB Egilsson, V Ingvarsson, S
Citation: Bi. Sigbjornsdottir et al., Chromosome 8p alterations in sporadic and BRCA2 999del5 linked breast cancer, J MED GENET, 37(5), 2000, pp. 342-347
Reduced Fhit expression in sporadic and BRCA2-linked breast carcinomas
Authors: Ingvarsson, S Agnarsson, BA Sigbjornsdottir, BI Kononen, J Kallioniemi, OP Barkardottir, RB Kovatich, AJ Schwarting, R Hauck, WW Huebner, K McCue, PA
Citation: S. Ingvarsson et al., Reduced Fhit expression in sporadic and BRCA2-linked breast carcinomas, CANCER RES, 59(11), 1999, pp. 2682-2689
European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables
Authors: Launonen, V Laake, K Huusko, P Niederacher, D Beckmann, MW Barkardottir, RB Geirsdottir, EK Gudmundsson, J Rio, P Bignon, YJ Seitz, S Scherneck, S Bieche, I Champeme, MH Birnbaum, D White, G Varley, J Sztan, M Olah, E Osorio, A Benitez, J Spurr, N Velikonja, N Peterlin, B Borg, A Cleton-Jansen, AM Devilee, P Bloigu, R Lidereau, R Borresen-Dale, AL Winqvist, R
Citation: V. Launonen et al., European multicenter study on LOH of APOC3 at 11q23 in 766 breast cancer patients: relation to clinical variables, BR J CANC, 80(5-6), 1999, pp. 879-882
Mapping lass of heterozygosity at chromosome 13q: Loss at 13q12-q13 is associated with breast tumour progression and poor prognosis
Authors: Eiriksdottir, G Johannesdottir, G Ingvarsson, S Bjornsdottir, IB Jonasson, JG Agnarsson, BA Hallgrimsson, J Gudmundsson, J Egilsson, V Sigurdsson, H Barkardottir, RB
Citation: G. Eiriksdottir et al., Mapping lass of heterozygosity at chromosome 13q: Loss at 13q12-q13 is associated with breast tumour progression and poor prognosis, EUR J CANC, 34(13), 1998, pp. 2076-2081
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
Risultati: 1-9 |