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118 related items for PubMed ID: 9043868

  • 1. Physical map and cosmid contig encompassing a new interstitial deletion of the X-linked lymphoproliferative syndrome region.
    Lamartine J, Nichols KE, Yin L, Krainer M, Heitzmann F, Bernard A, Gaudi S, Lenoir GM, Sullivan JL, Ikeda JE, Porta G, Schlessinger D, Romeo G, Haber DA, Sylla BS, Harkin DP.
    Eur J Hum Genet; 1996; 4(6):342-51. PubMed ID: 9043868
    [Abstract] [Full Text] [Related]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. A new candidate region for the positional cloning of the XLP gene.
    Bolino A, Yin L, Seri M, Cusano R, Cinti R, Coffey A, Brooksbank R, Howell G, Bentley D, Davis JR, Lanyi A, Huang D, Stark M, Creaven M, Bjørkhaug L, Heitzmann F, Lamartine J, Gaudi S, Sylla BS, Lenoir GM, Castagnola E, Giacchino R, Porta G, Franco B, Zollo M, Sumegi J, Romeo G.
    Eur J Hum Genet; 1998 Jan 01; 6(5):509-17. PubMed ID: 9801876
    [Abstract] [Full Text] [Related]

  • 4. High-resolution mapping of the X-linked lymphoproliferative syndrome region by FISH on combed DNA.
    Monier K, Michalet X, Lamartine J, Schurra C, Heitzmann F, Yin L, Cinti R, Sylla BS, Creaven M, Porta G, Vourc'h C, Robert-Nicoud M, Bensimon A, Romeo G.
    Cytogenet Cell Genet; 1998 Jan 01; 81(3-4):259-64. PubMed ID: 9730614
    [Abstract] [Full Text] [Related]

  • 5.
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  • 6. Physical mapping of Xq24-25 around loci closely linked to the X-linked lymphoproliferative syndrome locus: an overlapping YAC map and linkage between DXS12, DXS42, and DXS37.
    Wang Q, Ishikawa-Brush Y, Monaco AP, Nelson DL, Caskey CT, Pauly SP, Lenoir GM, Sylla BS.
    Eur J Hum Genet; 1993 Jan 01; 1(1):64-71. PubMed ID: 8069652
    [Abstract] [Full Text] [Related]

  • 7. Multipoint linkage mapping of the Xq25-q26 region in a family affected by the X-linked lymphoproliferative syndrome.
    Sylla BS, Wang Q, Hayoz D, Lathrop GM, Lenoir GM.
    Clin Genet; 1989 Dec 01; 36(6):459-62. PubMed ID: 2574086
    [Abstract] [Full Text] [Related]

  • 8. [X-chromosome recessive lymphoproliferative disease (XLP): molecular genetic studies].
    Schuster V, Grimm T, Kress W, Seidenspinner S, Belohradsky BH, Müller P, Kreth HW.
    Klin Padiatr; 1995 Dec 01; 207(5):271-6. PubMed ID: 7500602
    [Abstract] [Full Text] [Related]

  • 9. Chromosome deletion of Xq25 in an individual with X-linked lymphoproliferative disease.
    Wyandt HE, Grierson HL, Sanger WG, Skare JC, Milunsky A, Purtilo DT.
    Am J Med Genet; 1989 Jul 01; 33(3):426-30. PubMed ID: 2801783
    [Abstract] [Full Text] [Related]

  • 10. High-resolution mapping of probes near the X-linked lymphoproliferative disease (XLP) locus.
    Wu BL, Milunsky A, Nelson D, Schmeckpeper B, Porta G, Schlessinger D, Skare J.
    Genomics; 1993 Jul 01; 17(1):163-70. PubMed ID: 8406447
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  • 11.
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  • 12. Correlation of mutations of the SH2D1A gene and epstein-barr virus infection with clinical phenotype and outcome in X-linked lymphoproliferative disease.
    Sumegi J, Huang D, Lanyi A, Davis JD, Seemayer TA, Maeda A, Klein G, Seri M, Wakiguchi H, Purtilo DT, Gross TG.
    Blood; 2000 Nov 01; 96(9):3118-25. PubMed ID: 11049992
    [Abstract] [Full Text] [Related]

  • 13. A YAC-based binning strategy facilitating the rapid assembly of cosmid contigs: 1.6 Mb of overlapping cosmids in Xp22.
    Wapenaar MC, Schiaffino MV, Bassi MT, Schaefer L, Chinault AC, Zoghbi HY, Ballabio A.
    Hum Mol Genet; 1994 Jul 01; 3(7):1155-61. PubMed ID: 7981686
    [Abstract] [Full Text] [Related]

  • 14. Inactivating mutations in an SH2 domain-encoding gene in X-linked lymphoproliferative syndrome.
    Nichols KE, Harkin DP, Levitz S, Krainer M, Kolquist KA, Genovese C, Bernard A, Ferguson M, Zuo L, Snyder E, Buckler AJ, Wise C, Ashley J, Lovett M, Valentine MB, Look AT, Gerald W, Housman DE, Haber DA.
    Proc Natl Acad Sci U S A; 1998 Nov 10; 95(23):13765-70. PubMed ID: 9811875
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. Linkage analysis of seven kindreds with the X-linked lymphoproliferative syndrome (XLP) confirms that the XLP locus is near DXS42 and DXS37.
    Skare JC, Grierson HL, Sullivan JL, Nussbaum RL, Purtilo DT, Sylla BS, Lenoir GM, Reilly DS, White BN, Milunsky A.
    Hum Genet; 1989 Jul 15; 82(4):354-8. PubMed ID: 2567696
    [Abstract] [Full Text] [Related]

  • 17. X-linked lymphoproliferative disease is caused by deficiency of a novel SH2 domain-containing signal transduction adaptor protein.
    Schuster V, Kreth HW.
    Immunol Rev; 2000 Dec 15; 178():21-8. PubMed ID: 11213803
    [Abstract] [Full Text] [Related]

  • 18. X-linked lymphoproliferative disease: a karyotype analysis.
    Harris A, Docherty Z.
    Cytogenet Cell Genet; 1988 Dec 15; 47(1-2):92-4. PubMed ID: 2833379
    [Abstract] [Full Text] [Related]

  • 19. Construction of a 1-Mb restriction-mapped cosmid contig containing the candidate region for the familial Mediterranean fever locus (MEFV) on chromosome 16p 13.3.
    Sood R, Blake T, Aksentijevich I, Wood G, Chen X, Gardner D, Shelton DA, Mangelsdorf M, Orsborn A, Pras E, Balow JE, Centola M, Deng Z, Zaks N, Chen X, Richards N, Fischel-Ghodsian N, Rotter JI, Pras M, Shohat M, Deaven LL, Gumucio DL, Callen DF, Richards RI, Doggett NA.
    Genomics; 1997 May 15; 42(1):83-95. PubMed ID: 9177779
    [Abstract] [Full Text] [Related]

  • 20. Characterisation of molecular DNA rearrangements within the Xq12-q13.1 region, in three patients with X-linked hypohidrotic ectodermal dysplasia (EDA).
    Thomas NS, Chelly J, Zonana J, Davies KJ, Morgan S, Gault J, Rack KA, Buckle VJ, Brockdorff N, Clarke A.
    Hum Mol Genet; 1993 Oct 15; 2(10):1679-85. PubMed ID: 8268921
    [Abstract] [Full Text] [Related]

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