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Journal Abstract Search

397 related items for PubMed ID: 16024971

  • 1. Genomewide linkage scan in a multigeneration Caucasian pedigree identifies a novel locus for keratoconus on chromosome 5q14.3-q21.1.
    Tang YG, Rabinowitz YS, Taylor KD, Li X, Hu M, Picornell Y, Yang H.
    Genet Med; 2005; 7(6):397-405. PubMed ID: 16024971
    [Abstract] [Full Text] [Related]

  • 2. Apparent autosomal dominant keratoconus in a large Australian pedigree accounted for by digenic inheritance of two novel loci.
    Burdon KP, Coster DJ, Charlesworth JC, Mills RA, Laurie KJ, Giunta C, Hewitt AW, Latimer P, Craig JE.
    Hum Genet; 2008 Nov; 124(4):379-86. PubMed ID: 18795334
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  • 3. Two-stage genome-wide linkage scan in keratoconus sib pair families.
    Li X, Rabinowitz YS, Tang YG, Picornell Y, Taylor KD, Hu M, Yang H.
    Invest Ophthalmol Vis Sci; 2006 Sep; 47(9):3791-5. PubMed ID: 16936089
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  • 4. Genomewide linkage scan identifies a novel susceptibility locus for restless legs syndrome on chromosome 9p.
    Chen S, Ondo WG, Rao S, Li L, Chen Q, Wang Q.
    Am J Hum Genet; 2004 May; 74(5):876-85. PubMed ID: 15077200
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  • 5. Linkage analysis in keratoconus: replication of locus 5q21.2 and identification of other suggestive Loci.
    Bisceglia L, De Bonis P, Pizzicoli C, Fischetti L, Laborante A, Di Perna M, Giuliani F, Delle Noci N, Buzzonetti L, Zelante L.
    Invest Ophthalmol Vis Sci; 2009 Mar; 50(3):1081-6. PubMed ID: 18978346
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  • 8. Mapping a novel locus for familial atrial fibrillation on chromosome 10p11-q21.
    Volders PG, Zhu Q, Timmermans C, Eurlings PM, Su X, Arens YH, Li L, Jongbloed RJ, Xia M, Rodriguez LM, Chen YH.
    Heart Rhythm; 2007 Apr; 4(4):469-75. PubMed ID: 17399636
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  • 9. 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
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  • 14. A novel locus on 19q13 associated with autosomal-dominant macular dystrophy in a large Greek family.
    Yang Z, Kitsos G, Tong Z, Payne M, Gorezis S, Psilas K, Grigoriadou M, Zhao Y, Kamaya S, Aperis G, Petersen MB, Zhang K.
    J Med Genet; 2006 Dec 08; 43(12):e57. PubMed ID: 17142619
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  • 16. 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
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  • 17. Genome-wide linkage analysis of severe, early-onset chronic obstructive pulmonary disease: airflow obstruction and chronic bronchitis phenotypes.
    Silverman EK, Mosley JD, Palmer LJ, Barth M, Senter JM, Brown A, Drazen JM, Kwiatkowski DJ, Chapman HA, Campbell EJ, Province MA, Rao DC, Reilly JJ, Ginns LC, Speizer FE, Weiss ST.
    Hum Mol Genet; 2002 Mar 15; 11(6):623-32. PubMed ID: 11912177
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  • 18. Genomewide search for type 2 diabetes-susceptibility genes in French whites: evidence for a novel susceptibility locus for early-onset diabetes on chromosome 3q27-qter and independent replication of a type 2-diabetes locus on chromosome 1q21-q24.
    Vionnet N, Hani EH, Dupont S, Gallina S, Francke S, Dotte S, De Matos F, Durand E, Leprêtre F, Lecoeur C, Gallina P, Zekiri L, Dina C, Froguel P.
    Am J Hum Genet; 2000 Dec 15; 67(6):1470-80. PubMed ID: 11067779
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