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PUBMED FOR HANDHELDS

Journal Abstract Search


92 related items for PubMed ID: 14560309

  • 1. Genome-wide scanning for linkage in Finnish breast cancer families.
    Huusko P, Juo SH, Gillanders E, Sarantaus L, Kainu T, Vahteristo P, Allinen M, Jones M, Rapakko K, Eerola H, Markey C, Vehmanen P, Gildea D, Freas-Lutz D, Blomqvist C, Leisti J, Blanco G, Puistola U, Trent J, Bailey-Wilson J, Winqvist R, Nevanlinna H, Kallioniemi OP.
    Eur J Hum Genet; 2004 Feb; 12(2):98-104. PubMed ID: 14560309
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  • 2. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.
    Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797
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  • 3. 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; 16(1):135-41. PubMed ID: 15942690
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  • 4. No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 18q21.1.
    Sander T, Windemuth C, Schulz H, Saar K, Gennaro E, Bianchi A, Zara F, Bulteau C, Kaminska A, Ville D, Cieuta C, Prud'homme JF, Dulac O, Bate L, Gardiner RM, de Haan GJ, Janssen GA, Witte J, Halley DJ, Lindhout D, Wienker TF, Janz D, European Consortium on the Genetics of Idiopathic Generalized Epilepsy.
    Am J Med Genet; 2002 Aug 08; 114(6):673-8. PubMed ID: 12210286
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  • 10. Genome-wide scan for linkage in finnish hereditary prostate cancer (HPC) families identifies novel susceptibility loci at 11q14 and 3p25-26.
    Schleutker J, Baffoe-Bonnie AB, Gillanders E, Kainu T, Jones MP, Freas-Lutz D, Markey C, Gildea D, Riedesel E, Albertus J, Gibbs KD, Matikainen M, Koivisto PA, Tammela T, Bailey-Wilson JE, Trent JM, Kallioniemi OP.
    Prostate; 2003 Dec 01; 57(4):280-9. PubMed ID: 14601024
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  • 11. Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22.
    Rahman N, Teare MD, Seal S, Renard H, Mangion J, Cour C, Thompson D, Shugart Y, Eccles D, Devilee P, Meijers H, Nathanson KL, Neuhausen SL, Weber B, Chang-Claude J, Easton DF, Goldgar D, Stratton MR.
    Oncogene; 2000 Aug 24; 19(36):4170-3. PubMed ID: 10962578
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  • 15. Genome-wide scan for prostate cancer susceptibility genes in the Johns Hopkins hereditary prostate cancer families.
    Xu J, Gillanders EM, Isaacs SD, Chang BL, Wiley KE, Zheng SL, Jones M, Gildea D, Riedesel E, Albertus J, Freas-Lutz D, Markey C, Meyers DA, Walsh PC, Trent JM, Isaacs WB.
    Prostate; 2003 Dec 01; 57(4):320-5. PubMed ID: 14601028
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  • 16. Genetic epidemiology of breast cancer and associated cancers in high-risk families. II. Linkage analysis.
    King MC, Go RC, Lynch HT, Elston RC, Terasaki PI, Petrakis NL, Rodgers GC, Lattanzio D, Bailey-Wilson J.
    J Natl Cancer Inst; 1983 Sep 01; 71(3):463-7. PubMed ID: 6577221
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  • 17. A genome screen of 35 bipolar affective disorder pedigrees provides significant evidence for a susceptibility locus on chromosome 15q25-26.
    McAuley EZ, Blair IP, Liu Z, Fullerton JM, Scimone A, Van Herten M, Evans MR, Kirkby KC, Donald JA, Mitchell PB, Schofield PR.
    Mol Psychiatry; 2009 May 01; 14(5):492-500. PubMed ID: 18227837
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  • 18. Genomewide high-density SNP linkage analysis of non-BRCA1/2 breast cancer families identifies various candidate regions and has greater power than microsatellite studies.
    Gonzalez-Neira A, Rosa-Rosa JM, Osorio A, Gonzalez E, Southey M, Sinilnikova O, Lynch H, Oldenburg RA, van Asperen CJ, Hoogerbrugge N, Pita G, Devilee P, Goldgar D, Benitez J.
    BMC Genomics; 2007 Aug 30; 8():299. PubMed ID: 17760956
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  • 20. Fine mapping of the SLEB2 locus involved in susceptibility to systemic lupus erythematosus.
    Magnusson V, Lindqvist AK, Castillejo-López C, Kristjánsdottir H, Steinsson K, Gröndal G, Sturfelt G, Truedsson L, Svenungsson E, Lundberg I, Gunnarsson I, Bolstad AI, Haga HJ, Jonsson R, Klareskog L, Alcocer-Varela J, Alarcón-Segovia D, Terwilliger JD, Gyllensten UB, Alarcón-Riquelme ME.
    Genomics; 2000 Dec 15; 70(3):307-14. PubMed ID: 11161781
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