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Journal Abstract Search

142 related items for PubMed ID: 8449500

  • 1. Linkage analysis and physical mapping near the gene for X-linked agammaglobulinemia at Xq22.
    Parolini O, Hejtmancik JF, Allen RC, Belmont JW, Lassiter GL, Henry MJ, Barker DF, Conley ME.
    Genomics; 1993 Feb; 15(2):342-9. PubMed ID: 8449500
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  • 2. Identification of a closely linked DNA marker, DXS178, to further refine the X-linked agammaglobulinemia locus.
    Kwan SP, Terwilliger J, Parmley R, Raghu G, Sandkuyl LA, Ott J, Ochs H, Wedgwood R, Rosen F.
    Genomics; 1990 Feb; 6(2):238-42. PubMed ID: 2307467
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  • 3. Construction of a 5.2-megabase physical map of the human X chromosome at Xq22 using pulsed-field gel electrophoresis and yeast artificial chromosomes.
    Vetrie D, Bobrow M, Harris A.
    Genomics; 1993 Mar; 15(3):631-42. PubMed ID: 8096829
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  • 4. Isolation of cDNA clones mapping around DXS178: a search for human X-linked agammaglobulinaemia gene using yeast artificial chromosomes, cosmids and direct cDNA selection.
    Vorechovský I, Holland J, Sideras P, Dunham I, Hammarström L, Smith CI, Bentley DR, Vetrie D.
    Immunodeficiency; 1993 Mar; 4(1-4):221-4. PubMed ID: 8167705
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  • 10. Genetic linkage analysis identifies new proximal and distal flanking markers for the X-linked agammaglobulinemia gene locus, refining its localization in Xq22.
    Lovering R, Middleton-Price HR, O'Reilly MA, Genet SA, Parkar M, Sweatman AK, Bradley LD, Alterman LA, Malcolm S, Morgan G.
    Hum Mol Genet; 1993 Feb; 2(2):139-41. PubMed ID: 8499902
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  • 11. Physical mapping shows close linkage between the alpha-galactosidase A gene (GLA) and the DXS178 locus.
    Vetrie D, Bentley D, Bobrow M, Harris A.
    Hum Genet; 1993 Aug; 92(1):95-9. PubMed ID: 8103505
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  • 12. Mapping of the X-linked agammaglobulinemia locus by use of restriction fragment-length polymorphism.
    Kwan SP, Kunkel L, Bruns G, Wedgwood RJ, Latt S, Rosen FS.
    J Clin Invest; 1986 Feb; 77(2):649-52. PubMed ID: 3003164
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  • 13. A complete YAC contig and cosmid interval map covering the entirety of human Xq21.33 to Xq22.3 from DXS3 to DXS287.
    Kendall E, Evans W, Jin H, Holland J, Vetrie D.
    Genomics; 1997 Jul 15; 43(2):171-82. PubMed ID: 9244434
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  • 16. A yeast artificial chromosome (YAC) contig encompassing the critical region of the X-linked lymphoproliferative disease (XLP) locus.
    Lanyi A, Li B, Li S, Talmadge CB, Brichacek B, Davis JR, Kozel BA, Trask B, van den Engh G, Uzvolgyi E, Stanbridge EJ, Nelson DL, Chinault C, Heslop H, Gross TG, Seemayer TA, Klein G, Purtilo DT, Sumegi J.
    Genomics; 1997 Jan 01; 39(1):55-65. PubMed ID: 9027486
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  • 18. Close linkage of random DNA fragments from Xq 21.3-22 to X-linked agammaglobulinaemia (XLA).
    Malcolm S, de Saint Basile G, Arveiler B, Lau YL, Szabo P, Fischer A, Griscelli C, Debre M, Mandel JL, Callard RE.
    Hum Genet; 1987 Oct 01; 77(2):172-4. PubMed ID: 2888720
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  • 19. A 6.5-Mb yeast artificial chromosome contig incorporating 33 DNA markers on the human X chromosome at Xq22.
    Vetrie D, Kendall E, Coffey A, Hassock S, Collins J, Todd C, Lehrach H, Bobrow M, Bentley DR, Harris A.
    Genomics; 1994 Jan 01; 19(1):42-7. PubMed ID: 8188239
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  • 20. Fabry disease: molecular carrier detection and prenatal diagnosis by analysis of closely linked polymorphisms at Xq22.1.
    Caggana M, Ashley GA, Desnick RJ, Eng CM.
    Am J Med Genet; 1997 Aug 22; 71(3):329-35. PubMed ID: 9268104
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