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Journal Abstract Search

169 related items for PubMed ID: 11135493

  • 1. 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; 21(4):227-33. PubMed ID: 11135493
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  • 2. Autosomal dominant congenital nystagmus is not linked to 6p12, 7p11, and 15q11 in a German family.
    Hoffmann S, Becker A, Hoerle S, Metz A, Oertel WH, Sommer N, Hemmer B.
    Am J Ophthalmol; 2004 Sep; 138(3):439-43. PubMed ID: 15364228
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  • 3. A gene for autosomal dominant congenital nystagmus localizes to 6p12.
    Kerrison JB, Arnould VJ, Barmada MM, Koenekoop RK, Schmeckpeper BJ, Maumenee IH.
    Genomics; 1996 May 01; 33(3):523-6. PubMed ID: 8661013
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  • 5. 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 01; 16(1):33-8. PubMed ID: 11149487
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  • 10. 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 01; 152(1):29-36. PubMed ID: 15656797
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  • 18. A genome screen of 13 bipolar affective disorder pedigrees provides evidence for susceptibility loci on chromosome 3 as well as chromosomes 9, 13 and 19.
    Badenhop RF, Moses MJ, Scimone A, Mitchell PB, Ewen-White KR, Rosso A, Donald JA, Adams LJ, Schofield PR.
    Mol Psychiatry; 2002 Jan 01; 7(6):594-603. PubMed ID: 12140782
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  • 20. 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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