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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

159 related items for PubMed ID: 17760956

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  • 2. Familial concordance of breast cancer pathology as an indicator of genotype in multiple-case families.
    Balleine RL, Provan PJ, Pupo GM, Pathmanathan N, Cummings M, Farshid G, Salisbury EL, Bilous AM, Byth K, KConFab Investigators, Mann GJ.
    Genes Chromosomes Cancer; 2010 Dec; 49(12):1082-94. PubMed ID: 20815029
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  • 3. Linkage and association analyses of microsatellites and single-nucleotide polymorphisms in nuclear families.
    Lin J, Liu KY.
    BMC Genet; 2005 Dec 30; 6 Suppl 1(Suppl 1):S25. PubMed ID: 16451634
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  • 5. 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 30; 112(2):229-36. PubMed ID: 18095154
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  • 6. Genetic mapping of a 17q chromosomal region linked to obesity phenotypes in the IRAS family study.
    Sutton BS, Langefeld CD, Campbell JK, Haffner SM, Norris JM, Scherzinger AL, Wagenknecht LE, Bowden DW.
    Int J Obes (Lond); 2006 Sep 30; 30(9):1433-41. PubMed ID: 16520807
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  • 7. CGH analysis of familial non-BRCA1/BRCA2 breast tumors and mutation screening of a candidate locus on chromosome 17q11.2-12.
    Maguire P, Holmberg K, Kost-Alimova M, Imreh S, Skoog L, Lindblom A.
    Int J Mol Med; 2005 Jul 30; 16(1):135-41. PubMed ID: 15942690
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  • 8. A genome-wide linkage analysis of alcoholism on microsatellite and single-nucleotide polymorphism data, using alcohol dependence phenotypes and electroencephalogram measures.
    Zhang C, Cawley S, Liu G, Cao M, Gorrell H, Kennedy GC.
    BMC Genet; 2005 Dec 30; 6 Suppl 1(Suppl 1):S17. PubMed ID: 16451625
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  • 9. Prophylactic Oophorectomy: Reducing the U.S. Death Rate from Epithelial Ovarian Cancer. A Continuing Debate.
    Piver MS.
    Oncologist; 1996 Dec 30; 1(5):326-330. PubMed ID: 10388011
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  • 10. Characterization of familial non-BRCA1/2 breast tumors by loss of heterozygosity and immunophenotyping.
    Oldenburg RA, Kroeze-Jansema K, Meijers-Heijboer H, van Asperen CJ, Hoogerbrugge N, van Leeuwen I, Vasen HF, Cleton-Jansen AM, Kraan J, Houwing-Duistermaat JJ, Morreau H, Cornelisse CJ, Devilee P.
    Clin Cancer Res; 2006 Mar 15; 12(6):1693-700. PubMed ID: 16551851
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  • 11. Genome-wide linkage analysis for alcohol dependence: a comparison between single-nucleotide polymorphism and microsatellite marker assays.
    Ma Q, Yu Y, Meng Y, Farrell J, Farrer LA, Wilcox MA.
    BMC Genet; 2005 Dec 30; 6 Suppl 1(Suppl 1):S8. PubMed ID: 16451694
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  • 12. A 7 Mb region within 11q13 may contain a high penetrance gene for breast cancer.
    Rosa-Rosa JM, Pita G, González-Neira A, Milne RL, Fernandez V, Ruivenkamp C, van Asperen CJ, Devilee P, Benitez J.
    Breast Cancer Res Treat; 2009 Nov 30; 118(1):151-9. PubMed ID: 19205878
    [Abstract] [Full Text] [Related]

  • 13. Genome scan linkage analysis comparing microsatellites and single-nucleotide polymorphisms markers for two measures of alcoholism in chromosomes 1, 4, and 7.
    Chen G, Adeyemo A, Zhou J, Yuan A, Chen Y, Rotimi C.
    BMC Genet; 2005 Dec 30; 6 Suppl 1(Suppl 1):S4. PubMed ID: 16451650
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  • 19. Suggestive genetic linkage to chromosome 11p11.2-q12.2 in hereditary prostate cancer families with primary kidney cancer.
    Johanneson B, Deutsch K, McIntosh L, Friedrichsen-Karyadi DM, Janer M, Kwon EM, Iwasaki L, Hood L, Ostrander EA, Stanford JL.
    Prostate; 2007 May 15; 67(7):732-42. PubMed ID: 17372923
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