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131 related items for PubMed ID: 8069652

  • 1. 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; 1(1):64-71. PubMed ID: 8069652
    [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. 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
    [Abstract] [Full Text] [Related]

  • 4. 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 01; 82(4):354-8. PubMed ID: 2567696
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. Mapping the mutation causing the X-linked lymphoproliferative syndrome in relation to restriction fragment length polymorphisms on Xq.
    Skare JC, Sullivan JL, Milunsky A.
    Hum Genet; 1989 Jul 01; 82(4):349-53. PubMed ID: 2567695
    [Abstract] [Full Text] [Related]

  • 7. 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 Jul 01; 4(6):342-51. PubMed ID: 9043868
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  • 13. Walking, cloning, and mapping with yeast artificial chromosomes: a contig encompassing D21S13 and D21S16.
    Butler R, Ogilvie DJ, Elvin P, Riley JH, Finniear RS, Slynn G, Morten JE, Markham AF, Anand R.
    Genomics; 1992 Jan 01; 12(1):42-51. PubMed ID: 1733862
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  • 14. 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
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  • 15. Construction of a yeast artificial chromosome contig encompassing the human acidic fibroblast growth factor (FGF1) gene: toward the cloning of the ANLL/MDS tumor-suppressor gene.
    Chiu IM, Gilmore EC, Liu Y, Payson RA.
    Genomics; 1994 Feb 01; 19(3):552-60. PubMed ID: 7514571
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  • 16. 2.6 Mb YAC contig of the human X inactivation center region in Xq13: physical linkage of the RPS4X, PHKA1, XIST and DXS128E genes.
    Lafrenière RG, Brown CJ, Rider S, Chelly J, Taillon-Miller P, Chinault AC, Monaco AP, Willard HF.
    Hum Mol Genet; 1993 Aug 01; 2(8):1105-15. PubMed ID: 8401491
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  • 17. [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 Aug 01; 207(5):271-6. PubMed ID: 7500602
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  • 18. Lowe oculocerebrorenal syndrome in a female with a balanced X;20 translocation: mapping of the X chromosome breakpoint.
    Mueller OT, Hartsfield JK, Gallardo LA, Essig YP, Miller KL, Papenhausen PR, Tedesco TA.
    Am J Hum Genet; 1991 Oct 01; 49(4):804-10. PubMed ID: 1897526
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  • 19. High-resolution mapping by YAC fragmentation of a 2.5-Mb Xp22 region containing the human RS, KFSD and CLS disease genes.
    Van de Vosse E, Van der Bent P, Heus JJ, Van Ommen GJ, Den Dunnen JT.
    Mamm Genome; 1997 Jul 01; 8(7):497-501. PubMed ID: 9195994
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  • 20. A 2.3-Mb yeast artificial chromosome contig spanning from Gabra3 to G6pd on the mouse X chromosome.
    Chatterjee A, Faust CJ, Molinari-Storey L, Kiochis P, Poustka A, Herman GE.
    Genomics; 1994 May 01; 21(1):49-57. PubMed ID: 8088815
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