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PUBMED FOR HANDHELDS

Journal Abstract Search


249 related items for PubMed ID: 10208445

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  • 44. Genome-wide scan in Portuguese Island families implicates multiple loci in bipolar disorder: fine mapping adds support on chromosomes 6 and 11.
    Pato CN, Pato MT, Kirby A, Petryshen TL, Medeiros H, Carvalho C, Macedo A, Dourado A, Coelho I, Valente J, Soares MJ, Ferreira CP, Lei M, Verner A, Hudson TJ, Morley CP, Kennedy JL, Azevedo MH, Daly MJ, Sklar P.
    Am J Med Genet B Neuropsychiatr Genet; 2004 May 15; 127B(1):30-4. PubMed ID: 15108176
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  • 47. Genomewide scan in german families reveals evidence for a novel psoriasis-susceptibility locus on chromosome 19p13.
    Lee YA, Rüschendorf F, Windemuth C, Schmitt-Egenolf M, Stadelmann A, Nürnberg G, Ständer M, Wienker TF, Reis A, Traupe H.
    Am J Hum Genet; 2000 Oct 15; 67(4):1020-4. PubMed ID: 10986047
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  • 48. Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III.
    Levinson DF, Holmans P, Straub RE, Owen MJ, Wildenauer DB, Gejman PV, Pulver AE, Laurent C, Kendler KS, Walsh D, Norton N, Williams NM, Schwab SG, Lerer B, Mowry BJ, Sanders AR, Antonarakis SE, Blouin JL, DeLeuze JF, Mallet J.
    Am J Hum Genet; 2000 Sep 15; 67(3):652-63. PubMed ID: 10924404
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  • 50. Genome-wide scan of additional Jewish families confirms linkage of a myopia susceptibility locus to chromosome 22q12.
    Stambolian D, Ibay G, Reider L, Dana D, Moy C, Schlifka M, Holmes TN, Ciner E, Bailey-Wilson JE.
    Mol Vis; 2006 Dec 04; 12():1499-505. PubMed ID: 17167407
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  • 51. Linkage at 12q24 with systemic lupus erythematosus (SLE) is established and confirmed in Hispanic and European American families.
    Nath SK, Quintero-Del-Rio AI, Kilpatrick J, Feo L, Ballesteros M, Harley JB.
    Am J Hum Genet; 2004 Jan 04; 74(1):73-82. PubMed ID: 14658095
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  • 53. A genomewide linkage study of age at onset in schizophrenia.
    Cardno AG, Holmans PA, Rees MI, Jones LA, McCarthy GM, Hamshere ML, Williams NM, Norton N, Williams HJ, Fenton I, Murphy KC, Sanders RD, Gray MY, O'Donovan MC, McGuffin P, Owen MJ.
    Am J Med Genet; 2001 Jul 08; 105(5):439-45. PubMed ID: 11449396
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  • 54. Evidence for linkage of nonsyndromic cleft lip with or without cleft palate to a region on chromosome 2.
    Zeiger JS, Hetmanski JB, Beaty TH, VanderKolk CA, Wyszynski DF, Bailey-Wilson JE, de Luna RO, Perandones C, Tolarova MM, Mosby T, Bennun R, Segovia M, Calda P, Pugh EW, Doheny K, McIntosh I.
    Eur J Hum Genet; 2003 Nov 08; 11(11):835-9. PubMed ID: 14571267
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  • 57. Significant linkage to airway responsiveness on chromosome 12q24 in families of children with asthma in Costa Rica.
    Celedón JC, Soto-Quiros ME, Avila L, Lake SL, Liang C, Fournier E, Spesny M, Hersh CP, Sylvia JS, Hudson TJ, Verner A, Klanderman BJ, Freimer NB, Silverman EK, Weiss ST.
    Hum Genet; 2007 Jan 08; 120(5):691-9. PubMed ID: 17024367
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  • 60. A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2.
    Hoffmann K, Mattheisen M, Dahm S, Nürnberg P, Roe C, Johnson J, Cox NJ, Wichmann HE, Wienker TF, Schulze J, Schwarz PE, Lindner TH.
    Diabetologia; 2007 Jul 08; 50(7):1418-22. PubMed ID: 17464498
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