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Journal Abstract Search

263 related items for PubMed ID: 11149487

  • 1. Familial Paget's disease of bone: nonlinkage to the PDB1 and PDB2 loci on chromosomes 6p and 18q in a large pedigree.
    Good D, Busfield F, Duffy D, Lovelock PK, Kesting JB, Cameron DP, Shaw JT.
    J Bone Miner Res; 2001 Jan; 16(1):33-8. PubMed ID: 11149487
    [Abstract] [Full Text] [Related]

  • 2. Paget's disease of bone: evidence for a susceptibility locus on chromosome 18q and for genetic heterogeneity.
    Haslam SI, Van Hul W, Morales-Piga A, Balemans W, San-Millan JL, Nakatsuka K, Willems P, Haites NE, Ralston SH.
    J Bone Miner Res; 1998 Jun; 13(6):911-7. PubMed ID: 9626621
    [Abstract] [Full Text] [Related]

  • 3. Identification of a major locus for Paget's disease on chromosome 10p13 in families of British descent.
    Lucas GJ, Riches PL, Hocking LJ, Cundy T, Nicholson GC, Walsh JP, Ralston SH.
    J Bone Miner Res; 2008 Jan; 23(1):58-63. PubMed ID: 17907922
    [Abstract] [Full Text] [Related]

  • 4. Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease.
    Lee JH, Cheng R, Santana V, Williamson J, Lantigua R, Medrano M, Arriaga A, Stern Y, Tycko B, Rogaeva E, Wakutani Y, Kawarai T, St George-Hyslop P, Mayeux R.
    Arch Neurol; 2006 Nov; 63(11):1591-8. PubMed ID: 17101828
    [Abstract] [Full Text] [Related]

  • 5. Linkage of Paget disease of bone to a novel region on human chromosome 18q23.
    Good DA, Busfield F, Fletcher BH, Duffy DL, Kesting JB, Andersen J, Shaw JT.
    Am J Hum Genet; 2002 Feb; 70(2):517-25. PubMed ID: 11742440
    [Abstract] [Full Text] [Related]

  • 6. Inheritance of osteosarcoma and Paget's disease of bone: a familial loss of heterozygosity study.
    McNairn JD, Damron TA, Landas SK, Ambrose JL, Shrimpton AE.
    J Mol Diagn; 2001 Nov; 3(4):171-7. PubMed ID: 11687601
    [Abstract] [Full Text] [Related]

  • 7. Familial Paget's disease of bone: patterns of inheritance and frequency of linkage to chromosome 18q.
    Hocking L, Slee F, Haslam SI, Cundy T, Nicholson G, van Hul W, Ralston SH.
    Bone; 2000 Jun; 26(6):577-80. PubMed ID: 10831928
    [Abstract] [Full Text] [Related]

  • 8. Genome-wide scan of exfoliation syndrome.
    Lemmelä S, Forsman E, Sistonen P, Eriksson A, Forsius H, Järvelä I.
    Invest Ophthalmol Vis Sci; 2007 Sep; 48(9):4136-42. PubMed ID: 17724198
    [Abstract] [Full Text] [Related]

  • 9. A common locus for late-onset Fuchs corneal dystrophy maps to 18q21.2-q21.32.
    Sundin OH, Broman KW, Chang HH, Vito EC, Stark WJ, Gottsch JD.
    Invest Ophthalmol Vis Sci; 2006 Sep; 47(9):3919-26. PubMed ID: 16936105
    [Abstract] [Full Text] [Related]

  • 10. Further evidence of genetic heterogeneity segregating with hereditary gingival fibromatosis.
    Ye X, Shi L, Yin W, Meng L, Wang QK, Bian Z.
    J Clin Periodontol; 2009 Aug; 36(8):627-33. PubMed ID: 19552635
    [Abstract] [Full Text] [Related]

  • 11. Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort.
    Wilson SG, Adam G, Langdown M, Reneland R, Braun A, Andrew T, Surdulescu GL, Norberg M, Dudbridge F, Reed PW, Sambrook PN, Kleyn PW, Spector TD.
    Eur J Hum Genet; 2006 Mar; 14(3):340-8. PubMed ID: 16391564
    [Abstract] [Full Text] [Related]

  • 12. 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
    [Abstract] [Full Text] [Related]

  • 13. Genetic linkage mapping for a susceptibility locus to bipolar illness: chromosomes 2, 3, 4, 7, 9, 10p, 11p, 22, and Xpter.
    Detera-Wadleigh SD, Hsieh WT, Berrettini WH, Goldin LR, Rollins DY, Muniec D, Grewal R, Guroff JJ, Turner G, Coffman D.
    Am J Med Genet; 1994 Sep 15; 54(3):206-18. PubMed ID: 7810578
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  • 16. Evidence for genetic heterogeneity in families with congenital motor nystagmus (CN).
    Oetting WS, Armstrong CM, Holleschau AM, DeWan AT, Summers GC.
    Ophthalmic Genet; 2000 Dec 15; 21(4):227-33. PubMed ID: 11135493
    [Abstract] [Full Text] [Related]

  • 17. Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?
    Lohmann-Hedrich K, Neumann A, Kleensang A, Lohnau T, Muhle H, Djarmati A, König IR, Pramstaller PP, Schwinger E, Kramer PL, Ziegler A, Stephani U, Klein C.
    Neurology; 2008 Feb 26; 70(9):686-94. PubMed ID: 18032746
    [Abstract] [Full Text] [Related]

  • 18. Exclusion of an extracolonic disease modifier locus on chromosome 1p33-36 in a large Swiss familial adenomatous polyposis kindred.
    Plasilova M, Russell AM, Wanner A, Wolf A, Dobbie Z, Müller HJ, Heinimann K.
    Eur J Hum Genet; 2004 May 26; 12(5):365-71. PubMed ID: 14735163
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  • 20. Genetic linkage of familial expansile osteolysis to chromosome 18q.
    Hughes AE, Shearman AM, Weber JL, Barr RJ, Wallace RG, Osterberg PH, Nevin NC, Mollan RA.
    Hum Mol Genet; 1994 Feb 26; 3(2):359-61. PubMed ID: 7911698
    [Abstract] [Full Text] [Related]

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