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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

116 related items for PubMed ID: 22218795

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  • 2. [Genetic predisposition for breast cancer: BRCA1 and BRCA2 genes].
    Narod SA, Rodríguez AA.
    Salud Publica Mex; 2011; 53(5):420-9. PubMed ID: 22218796
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  • 6. Italian family with two independent mutations: 3358T/A in BRCA1 and 8756delA in BRCA2 genes.
    Cortesi L, Turchetti D, Bertoni C, Zanocco-Marani T, Vinceti M, Silvestri C, Federico M, Silingardi V, Ferrari S.
    Eur J Hum Genet; 2003 Mar; 11(3):210-4. PubMed ID: 12673274
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  • 9. Hereditary breast cancer: high risk genes, genetic testing and clinical implications.
    Hamann U.
    Clin Lab; 2000 Mar; 46(9-10):447-61. PubMed ID: 11034530
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  • 10. Breast cancer risk associated with BRCA1 and BRCA2 in diverse populations.
    Fackenthal JD, Olopade OI.
    Nat Rev Cancer; 2007 Dec; 7(12):937-48. PubMed ID: 18034184
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  • 12. [Risk assessment for familial occurrence of breast cancer].
    Chang-Claude J, Becher H, Hamann U, Schroeder-Kurth T.
    Zentralbl Gynakol; 1995 Dec; 117(8):423-34. PubMed ID: 7571905
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  • 14. Sex ratio distortion in offspring of families with BRCA1 or BRCA2 mutant alleles: an ascertainment bias phenomenon?
    Balmaña J, Díez O, Campos B, Majewski M, Sanz J, Alonso C, Baiget M, Garber JE.
    Breast Cancer Res Treat; 2005 Aug; 92(3):273-7. PubMed ID: 16155798
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  • 15. Analysis of FANCB and FANCN/PALB2 fanconi anemia genes in BRCA1/2-negative Spanish breast cancer families.
    García MJ, Fernández V, Osorio A, Barroso A, Llort G, Lázaro C, Blanco I, Caldés T, de la Hoya M, Ramón Y Cajal T, Alonso C, Tejada MI, San Román C, Robles-Díaz L, Urioste M, Benítez J.
    Breast Cancer Res Treat; 2009 Feb; 113(3):545-51. PubMed ID: 18302019
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  • 16. Hereditary breast cancer syndromes and clinical implications.
    Majdak-Paredes EJ, Fatah F.
    J Plast Reconstr Aesthet Surg; 2009 Feb; 62(2):181-9. PubMed ID: 19027378
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  • 17. Cancer risk assessment and the genetic counseling process: using hereditary breast and ovarian cancer as an example.
    Prucka SK, McIlvried DE, Korf BR.
    Med Princ Pract; 2008 Feb; 17(3):173-89. PubMed ID: 18408385
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  • 18. Hereditary breast cancer.
    Hill AD, Doyle JM, McDermott EW, O'Higgins NJ.
    Br J Surg; 1997 Oct; 84(10):1334-9. PubMed ID: 9361585
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  • 20. Use of expression data and the CGEMS genome-wide breast cancer association study to identify genes that may modify risk in BRCA1/2 mutation carriers.
    Walker LC, Waddell N, Ten Haaf A, kConFab Investigators, Grimmond S, Spurdle AB.
    Breast Cancer Res Treat; 2008 Nov; 112(2):229-36. PubMed ID: 18095154
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