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Journal Abstract Search

435 related items for PubMed ID: 20637093

  • 1. Genome-wide search for breast cancer linkage in large Icelandic non-BRCA1/2 families.
    Arason A, Gunnarsson H, Johannesdottir G, Jonasson K, Bendahl PO, Gillanders EM, Agnarsson BA, Jönsson G, Pylkäs K, Mustonen A, Heikkinen T, Aittomäki K, Blomqvist C, Melin B, Johannsson OT, Møller P, Winqvist R, Nevanlinna H, Borg A, Barkardottir RB.
    Breast Cancer Res; 2010; 12(4):R50. PubMed ID: 20637093
    [Abstract] [Full Text] [Related]

  • 2. Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus.
    Kainu T, Juo SH, Desper R, Schaffer AA, Gillanders E, Rozenblum E, Freas-Lutz D, Weaver D, Stephan D, Bailey-Wilson J, Kallioniemi OP, Tirkkonen M, Syrjäkoski K, Kuukasjärvi 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, Grönberg H, Olsson H, Borg A, Vehmanen P, Eerola H, Heikkila P, Pyrhönen S, Nevanlinna H.
    Proc Natl Acad Sci U S A; 2000 Aug 15; 97(17):9603-8. PubMed ID: 10944226
    [Abstract] [Full Text] [Related]

  • 3. Genome-wide linkage scan in Dutch hereditary non-BRCA1/2 breast cancer families identifies 9q21-22 as a putative breast cancer susceptibility locus.
    Oldenburg RA, Kroeze-Jansema KH, Houwing-Duistermaat JJ, Bayley JP, Dambrot C, van Asperen CJ, van den Ouweland AM, Bakker B, van Beers EH, Nederlof PM, Vasen H, Hoogerbrugge N, Cornelisse CJ, Meijers-Heijboer H, Devilee P.
    Genes Chromosomes Cancer; 2008 Nov 15; 47(11):947-56. PubMed ID: 18663745
    [Abstract] [Full Text] [Related]

  • 4. Whole-genome Linkage Analysis and Sequence Analysis of Candidate Loci in Familial Breast Cancer.
    Marikkannu R, Aravidis C, Rantala J, Picelli S, Adamovic T, Keihas M, Liu T, Kontham V, Nilsson D, Lindblom A.
    Anticancer Res; 2015 Jun 15; 35(6):3155-65. PubMed ID: 26026075
    [Abstract] [Full Text] [Related]

  • 5. A genome-wide analysis in consanguineous families reveals new chromosomal loci in specific language impairment (SLI).
    Andres EM, Hafeez H, Yousaf A, Riazuddin S, Rice ML, Basra MAR, Raza MH.
    Eur J Hum Genet; 2019 Aug 15; 27(8):1274-1285. PubMed ID: 30976110
    [Abstract] [Full Text] [Related]

  • 6. Genome-wide linkage scan reveals three putative breast-cancer-susceptibility loci.
    Rosa-Rosa JM, Pita G, Urioste M, Llort G, Brunet J, Lázaro C, Blanco I, Ramón y Cajal T, Díez O, de la Hoya M, Caldés T, Tejada MI, González-Neira A, Benítez J.
    Am J Hum Genet; 2009 Feb 15; 84(2):115-22. PubMed ID: 19147119
    [Abstract] [Full Text] [Related]

  • 7. Genome-wide linkage analysis reveals evidence for four new susceptibility loci for familial euthyroid goiter.
    Bayer Y, Neumann S, Meyer B, Rüschendorf F, Reske A, Brix T, Hegedüs L, Langer P, Nürnberg P, Paschke R.
    J Clin Endocrinol Metab; 2004 Aug 15; 89(8):4044-52. PubMed ID: 15292347
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. Fine mapping and SNP analysis of positional candidates at the preeclampsia susceptibility locus (PREG1) on chromosome 2.
    Fitzpatrick E, Göring HH, Liu H, Borg A, Forrest S, Cooper DW, Brennecke SP, Moses EK.
    Hum Biol; 2004 Dec 15; 76(6):849-62. PubMed ID: 15974297
    [Abstract] [Full Text] [Related]

  • 10. Linkage analysis of candidate regions in Swedish nonsyndromic cleft lip with or without cleft palate families.
    Wong FK, Hagberg C, Karsten A, Larson O, Gustavsson M, Huggare J, Larsson C, Teh BT, Linder-Aronson S.
    Cleft Palate Craniofac J; 2000 Jul 15; 37(4):357-62. PubMed ID: 10912714
    [Abstract] [Full Text] [Related]

  • 11. 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 15; 16(1):135-41. PubMed ID: 15942690
    [Abstract] [Full Text] [Related]

  • 12. A second-generation genomic screen for multiple sclerosis.
    Kenealy SJ, Babron MC, Bradford Y, Schnetz-Boutaud N, Haines JL, Rimmler JB, Schmidt S, Pericak-Vance MA, Barcellos LF, Lincoln RR, Oksenberg JR, Hauser SL, Clanet M, Brassat D, Edan G, Yaouanq J, Semana G, Cournu-Rebeix I, Lyon-Caen O, Fontaine B, American-French Multiple Sclerosis Genetics Group.
    Am J Hum Genet; 2004 Dec 15; 75(6):1070-8. PubMed ID: 15494893
    [Abstract] [Full Text] [Related]

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  • 14. Linkage genome scan for loci predisposing to panic disorder or agoraphobia.
    Gelernter J, Bonvicini K, Page G, Woods SW, Goddard AW, Kruger S, Pauls DL, Goodson S.
    Am J Med Genet; 2001 Aug 08; 105(6):548-57. PubMed ID: 11496373
    [Abstract] [Full Text] [Related]

  • 15. Locus heterogeneity, anticipation and reduction of the chromosome 2p minimal candidate region in autosomal dominant familial spastic paraplegia.
    Scott WK, Gaskell PC, Lennon F, Wolpert CM, Menold MM, Aylsworth AS, Warner C, Farrell CD, Boustany RM, Albright SG, Boyd E, Kingston HM, Cumming WJ, Vance JM, Pericak-Vance MA.
    Neurogenetics; 1997 Sep 08; 1(2):95-102. PubMed ID: 10732810
    [Abstract] [Full Text] [Related]

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  • 17. A genome wide linkage analysis in Swedish families with hereditary non-familial adenomatous polyposis/non-hereditary non-polyposis colorectal cancer.
    Djureinovic T, Skoglund J, Vandrovcova J, Zhou XL, Kalushkova A, Iselius L, Lindblom A.
    Gut; 2006 Mar 08; 55(3):362-6. PubMed ID: 16150854
    [Abstract] [Full Text] [Related]

  • 18. A genome-wide search for linkage to asthma phenotypes in the genetics of asthma international network families: evidence for a major susceptibility locus on chromosome 2p.
    Pillai SG, Chiano MN, White NJ, Speer M, Barnes KC, Carlsen K, Gerritsen J, Helms P, Lenney W, Silverman M, Sly P, Sundy J, Tsanakas J, von Berg A, Whyte M, Varsani S, Skelding P, Hauser M, Vance J, Pericak-Vance M, Burns DK, Middleton LT, Brewster SR, Anderson WH, Riley JH.
    Eur J Hum Genet; 2006 Mar 08; 14(3):307-16. PubMed ID: 16391567
    [Abstract] [Full Text] [Related]

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  • 20. Genome-wide linkage scan of a large family with IgA nephropathy localizes a novel susceptibility locus to chromosome 2q36.
    Paterson AD, Liu XQ, Wang K, Magistroni R, Song X, Kappel J, Klassen J, Cattran D, St George-Hyslop P, Pei Y.
    J Am Soc Nephrol; 2007 Aug 08; 18(8):2408-15. PubMed ID: 17634434
    [Abstract] [Full Text] [Related]

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