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Journal Abstract Search

58 related items for PubMed ID: 15300623

  • 21. A new locus for inherited nuclear cataract mapped to the long arm of chromosome 1.
    Wang L, Lin H, Shen Y, Huang S, Gu J, Su H, Qi Y.
    Mol Vis; 2007 Aug 01; 13():1357-62. PubMed ID: 17768382
    [Abstract] [Full Text] [Related]

  • 22. Interleukin 1 polymorphisms in patients with ankylosing spondylitis in Korea.
    Kim TJ, Kim TH, Lee HJ, Peddle L, Rahman P, Hu P, Greenwood CM, Inman RD.
    J Rheumatol; 2008 Aug 01; 35(8):1603-8. PubMed ID: 18484691
    [Abstract] [Full Text] [Related]

  • 23. Localization of a susceptibility locus for hepatocellular carcinoma to chromosome 4q in a hepatitis B hyperendemic area.
    Shih WL, Yu MW, Chen PJ, Yeh SH, Lo MT, Chang HC, Liaw YF, Lin SM, Liu CJ, Lee SD, Lin CL, Hsiao CK, Yang SY, Chen CJ.
    Oncogene; 2006 May 25; 25(22):3219-24. PubMed ID: 16407824
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  • 24. Objective prioritization of positional candidate genes at a quantitative trait locus for pre-eclampsia on 2q22.
    Moses EK, Fitzpatrick E, Freed KA, Dyer TD, Forrest S, Elliott K, Johnson MP, Blangero J, Brennecke SP.
    Mol Hum Reprod; 2006 Aug 25; 12(8):505-12. PubMed ID: 16809377
    [Abstract] [Full Text] [Related]

  • 25. Association of chromosome 2q36.1-36.3 and autosomal dominant transmission in ankylosing spondylitis: results of genetic studies across generations of Han Chinese families.
    Gu J, Huang J, Li C, Zhao L, Huang F, Liao Z, Li T, Wei Q, Lin Z, Pan Y, Huang J, Wang X, Lin Q, Lu C, Wu Y, Cao S, Wu J, Xu H, Yu B, Shen Y.
    J Med Genet; 2009 Oct 25; 46(10):657-62. PubMed ID: 19416804
    [Abstract] [Full Text] [Related]

  • 26. Further evidence for linkage of familial hyperaldosteronism type II at chromosome 7p22 in Italian as well as Australian and South American families.
    Sukor N, Mulatero P, Gordon RD, So A, Duffy D, Bertello C, Kelemen L, Jeske Y, Veglio F, Stowasser M.
    J Hypertens; 2008 Aug 25; 26(8):1577-82. PubMed ID: 18622235
    [Abstract] [Full Text] [Related]

  • 27. [A related analysis for alpha, beta fibrinogen gene haplotypes and nucleotide polymorphisms associated with the ischemic stroke in Hainan Han population].
    Liang L, Sun C, Liao XP, Xiao F, Chen XD, Huang SX, Tang XL, Wen GQ, Long ZG, Wang XY, Liu GX, Cheng S, Cai WW.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2006 Jun 25; 23(3):316-9. PubMed ID: 16767673
    [Abstract] [Full Text] [Related]

  • 28. A haplotype within the DISC1 gene is associated with visual memory functions in families with a high density of schizophrenia.
    Hennah W, Tuulio-Henriksson A, Paunio T, Ekelund J, Varilo T, Partonen T, Cannon TD, Lönnqvist J, Peltonen L.
    Mol Psychiatry; 2005 Dec 25; 10(12):1097-103. PubMed ID: 16103888
    [Abstract] [Full Text] [Related]

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  • 34. Association of a TNAP haplotype with ankylosing spondylitis.
    Tsui HW, Inman RD, Reveille JD, Tsui FW.
    Arthritis Rheum; 2007 Jan 25; 56(1):234-43. PubMed ID: 17195227
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  • 35. Multiple alpha-synuclein gene polymorphisms are associated with Parkinson's disease in a Norwegian population.
    Myhre R, Toft M, Kachergus J, Hulihan MM, Aasly JO, Klungland H, Farrer MJ.
    Acta Neurol Scand; 2008 Nov 25; 118(5):320-7. PubMed ID: 18485051
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  • 36. [Progress on genetic susceptibility to ankylosing spondylitis].
    Chen RW, Wang Y, Sun SH, Duan SW.
    Yi Chuan Xue Bao; 2005 Oct 25; 32(10):1108-14. PubMed ID: 16252708
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  • 37. ANKH variants associated with ankylosing spondylitis: gender differences.
    Tsui HW, Inman RD, Paterson AD, Reveille JD, Tsui FW.
    Arthritis Res Ther; 2005 Oct 25; 7(3):R513-25. PubMed ID: 15899038
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  • 39. [Increased incidence of chromosome anomalies in a family with ankylosing spondylitis].
    Olinici CD, Boloşiu HD.
    Rev Med Interna Neurol Psihiatr Neurochir Dermatovenerol Med Interna; 1977 Oct 25; 29(2):189-92. PubMed ID: 17912
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