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4. A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes. Thorlacius S; Olafsdottir G; Tryggvadottir L; Neuhausen S; Jonasson JG; Tavtigian SV; Tulinius H; Ogmundsdottir HM; Eyfjörd JE Nat Genet; 1996 May; 13(1):117-9. PubMed ID: 8673089 [TBL] [Abstract][Full Text] [Related]
5. Haplotype analysis of the BRCA2 9254delATCAT recurrent mutation in breast/ovarian cancer families from Spain. Campos B; Díez O; Odefrey F; Domènech M; Moncoutier V; Martínez-Ferrandis JI; Osorio A; Balmaña J; Barroso A; Armengod ME; Benítez J; Alonso C; Stoppa-Lyonnet D; Goldgar D; Baiget M Hum Mutat; 2003 Apr; 21(4):452. PubMed ID: 12655574 [TBL] [Abstract][Full Text] [Related]
6. Population-based study of changing breast cancer risk in Icelandic BRCA2 mutation carriers, 1920-2000. Tryggvadottir L; Sigvaldason H; Olafsdottir GH; Jonasson JG; Jonsson T; Tulinius H; Eyfjörd JE J Natl Cancer Inst; 2006 Jan; 98(2):116-22. PubMed ID: 16418514 [TBL] [Abstract][Full Text] [Related]
7. Haplotype analysis suggest common founders in carriers of the recurrent BRCA2 mutation, 3398delAAAAG, in French Canadian hereditary breast and/ovarian cancer families. Oros KK; Leblanc G; Arcand SL; Shen Z; Perret C; Mes-Masson AM; Foulkes WD; Ghadirian P; Provencher D; Tonin PN BMC Med Genet; 2006 Mar; 7():23. PubMed ID: 16539696 [TBL] [Abstract][Full Text] [Related]
8. High prevalence of the 999del5 mutation in icelandic breast and ovarian cancer patients. Johannesdottir G; Gudmundsson J; Bergthorsson JT; Arason A; Agnarsson BA; Eiriksdottir G; Johannsson OT; Borg A; Ingvarsson S; Easton DF; Egilsson V; Barkardottir RB Cancer Res; 1996 Aug; 56(16):3663-5. PubMed ID: 8706004 [TBL] [Abstract][Full Text] [Related]
9. A low proportion of BRCA2 mutations in Finnish breast cancer families. Vehmanen P; Friedman LS; Eerola H; Sarantaus L; Pyrhönen S; Ponder BA; Muhonen T; Nevanlinna H Am J Hum Genet; 1997 May; 60(5):1050-8. PubMed ID: 9150152 [TBL] [Abstract][Full Text] [Related]
10. The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplotype of today is a reminiscence of a 1500-year-old mutation. Bergman A; Einbeigi Z; Olofsson U; Taib Z; Wallgren A; Karlsson P; Wahlström J; Martinsson T; Nordling M Eur J Hum Genet; 2001 Oct; 9(10):787-93. PubMed ID: 11781691 [TBL] [Abstract][Full Text] [Related]
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12. Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BACH1 among BRCA1 and BRCA2-negative probands from breast-ovarian cancer families and among early-onset breast cancer cases and reference individuals. Rutter JL; Smith AM; Dávila MR; Sigurdson AJ; Giusti RM; Pineda MA; Doody MM; Tucker MA; Greene MH; Zhang J; Struewing JP Hum Mutat; 2003 Aug; 22(2):121-8. PubMed ID: 12872252 [TBL] [Abstract][Full Text] [Related]
13. BRCA2 founder mutation in Slovenian breast cancer families. Krajc M; De Grève J; Goelen G; Teugels E Eur J Hum Genet; 2002 Dec; 10(12):879-82. PubMed ID: 12461697 [TBL] [Abstract][Full Text] [Related]
14. Screening for a BRCA2 rearrangement in high-risk breast/ovarian cancer families: evidence for a founder effect and analysis of the associated phenotypes. Machado PM; Brandão RD; Cavaco BM; Eugénio J; Bento S; Nave M; Rodrigues P; Fernandes A; Vaz F J Clin Oncol; 2007 May; 25(15):2027-34. PubMed ID: 17513806 [TBL] [Abstract][Full Text] [Related]
15. The Icelandic founder mutation BRCA2 999del5: analysis of expression. Mikaelsdottir EK; Valgeirsdottir S; Eyfjord JE; Rafnar T Breast Cancer Res; 2004; 6(4):R284-90. PubMed ID: 15217494 [TBL] [Abstract][Full Text] [Related]
16. Incidence of BRCA1 and BRCA2 mutations in 54 Chilean families with breast/ovarian cancer, genotype-phenotype correlations. Gallardo M; Silva A; Rubio L; Alvarez C; Torrealba C; Salinas M; Tapia T; Faundez P; Palma L; Riccio ME; Paredes H; Rodriguez M; Cruz A; Rousseau C; King MC; Camus M; Alvarez M; Carvallo P Breast Cancer Res Treat; 2006 Jan; 95(1):81-7. PubMed ID: 16261400 [TBL] [Abstract][Full Text] [Related]
17. Prostate cancer progression and survival in BRCA2 mutation carriers. Tryggvadóttir L; Vidarsdóttir L; Thorgeirsson T; Jonasson JG; Olafsdóttir EJ; Olafsdóttir GH; Rafnar T; Thorlacius S; Jonsson E; Eyfjord JE; Tulinius H J Natl Cancer Inst; 2007 Jun; 99(12):929-35. PubMed ID: 17565157 [TBL] [Abstract][Full Text] [Related]
18. Usefulness of polymorphic markers in exclusion of BRCA1/BRCA2 mutations in families with aggregation of breast/ovarian cancers. Górski B; Debniak T; Jakubowska A; Cybulski C; Huzarski T; Byrski T; Złowocka E; Lubiński J J Appl Genet; 2003; 44(3):419-23. PubMed ID: 12923317 [TBL] [Abstract][Full Text] [Related]
19. Analysis of BRCA1 and BRCA2 genes in Spanish breast/ovarian cancer patients: a high proportion of mutations unique to Spain and evidence of founder effects. Díez O; Osorio A; Durán M; Martinez-Ferrandis JI; de la Hoya M; Salazar R; Vega A; Campos B; Rodríguez-López R; Velasco E; Chaves J; Díaz-Rubio E; Jesús Cruz J; Torres M; Esteban E; Cervantes A; Alonso C; San Román JM; González-Sarmiento R; Miner C; Carracedo A; Eugenia Armengod M; Caldés T; Benítez J; Baiget M Hum Mutat; 2003 Oct; 22(4):301-12. PubMed ID: 12955716 [TBL] [Abstract][Full Text] [Related]
20. Origin and distribution of the BRCA2-8765delAG mutation in breast cancer. Palomba G; Cossu A; Friedman E; Budroni M; Farris A; Contu A; Pisano M; Baldinu P; Sini MC; Tanda F; Palmieri G BMC Cancer; 2007 Jul; 7():132. PubMed ID: 17640379 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]