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86 related items for PubMed ID: 8406447

  • 1. 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; 17(1):163-70. PubMed ID: 8406447
    [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. 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]

  • 4. 4.5-Mb YAC STS contig at 50-kb resolution, spanning Xq25 deletions in two patients with lymphoproliferative syndrome.
    Porta G, MacMillan S, Nagaraja R, Mumm S, Zucchi I, Pilia G, Maio S, Featherstone T, Schlessinger D.
    Genome Res; 1997 Jan 01; 7(1):27-36. PubMed ID: 9037599
    [Abstract] [Full Text] [Related]

  • 5. 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]

  • 6. [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 Jul 01; 207(5):271-6. PubMed ID: 7500602
    [Abstract] [Full Text] [Related]

  • 7. X-linked lymphoproliferative disease: prenatal detection of an unaffected histocompatible male.
    Mulley JC, Turner AM, Gedeon AK, Berdoukas VA, Huang TH, Ledbetter DH, Grierson H, Purtilo DT.
    Clin Genet; 1992 Aug 01; 42(2):76-9. PubMed ID: 1358486
    [Abstract] [Full Text] [Related]

  • 8. Characterization of three overlapping deletions causing X-linked lymphoproliferative disease.
    Skare J, Wu BL, Madan S, Pulijaal V, Purtilo D, Haber D, Nelson D, Sylla B, Grierson H, Nitowsky H.
    Genomics; 1993 Apr 01; 16(1):254-5. PubMed ID: 8387453
    [Abstract] [Full Text] [Related]

  • 9. Genetic and physical mapping of Xq24-q26 markers flanking the Lowe oculocerebrorenal syndrome.
    Reilly DS, Lewis RA, Nussbaum RL.
    Genomics; 1990 Sep 01; 8(1):62-70. PubMed ID: 2081601
    [Abstract] [Full Text] [Related]

  • 10. Characterization of a highly complex region in Xq13 and mapping of three isodicentric breakpoints associated with preleukemia.
    McDonell N, Ramser J, Francis F, Vinet MC, Rider S, Sudbrak R, Riesselman L, Yaspo ML, Reinhardt R, Monaco AP, Ross F, Kahn A, Kearney L, Buckle V, Chelly J.
    Genomics; 2000 Mar 15; 64(3):221-9. PubMed ID: 10756090
    [Abstract] [Full Text] [Related]

  • 11. Partial Xq25 deletion in a family with the X-linked lymphoproliferative disease (XLP).
    Sanger WG, Grierson HL, Skare J, Wyandt H, Pirruccello S, Fordyce R, Purtilo DT.
    Cancer Genet Cytogenet; 1990 Jul 15; 47(2):163-9. PubMed ID: 1972651
    [Abstract] [Full Text] [Related]

  • 12. 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 Jul 15; 81(3-4):259-64. PubMed ID: 9730614
    [Abstract] [Full Text] [Related]

  • 13. Delineation by molecular cytogenetics of 5q deletion breakpoints in myelodyplastic syndromes and acute myeloid leukemia.
    Royer-Pokora B, Trost D, Müller N, Hildebrandt B, Germing U, Beier M.
    Cancer Genet Cytogenet; 2006 May 15; 167(1):66-9. PubMed ID: 16682289
    [Abstract] [Full Text] [Related]

  • 14. Fine structure mapping of the hypoxanthine-guanine phosphoribosyltransferase (HPRT) gene region of the human X chromosome (Xq26).
    Nicklas JA, Hunter TC, O'Neill JP, Albertini RJ.
    Am J Hum Genet; 1991 Aug 15; 49(2):267-78. PubMed ID: 1678246
    [Abstract] [Full Text] [Related]

  • 15. 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]

  • 16. Increased gene dosage at Xq26-q27 is associated with X-linked hypopituitarism.
    Solomon NM, Nouri S, Warne GL, Lagerström-Fermér M, Forrest SM, Thomas PQ.
    Genomics; 2002 Apr 15; 79(4):553-9. PubMed ID: 11944988
    [Abstract] [Full Text] [Related]

  • 17. Localization of deletion to a 300 Kb interval of chromosome 11q13 in cervical cancer.
    Srivatsan ES, Chakrabarti R, Zainabadi K, Pack SD, Benyamini P, Mendonca MS, Yang PK, Kang K, Motamedi D, Sawicki MP, Zhuang Z, Jesudasan RA, Bengtsson U, Sun C, Roe BA, Stanbridge EJ, Wilczynski SP, Redpath JL.
    Oncogene; 2002 Aug 15; 21(36):5631-42. PubMed ID: 12165862
    [Abstract] [Full Text] [Related]

  • 18. Fluorescence in situ hybridization deletion mapping at 4p16.3 in bladder cancer cell lines refines the localisation of the critical interval to 30 kb.
    Bell SM, Zuo J, Myers RM, Knowles MA.
    Genes Chromosomes Cancer; 1996 Oct 15; 17(2):108-17. PubMed ID: 8913728
    [Abstract] [Full Text] [Related]

  • 19. 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 15; 36(6):459-62. PubMed ID: 2574086
    [Abstract] [Full Text] [Related]

  • 20. A fluorescence in situ hybridization map of human chromosome 21 consisting of 30 genetic and physical markers on the chromosome: localization of 137 additional YAC and cosmid clones with respect to this map.
    Gingrich JC, Shadravan F, Lowry SR.
    Genomics; 1993 Jul 15; 17(1):98-105. PubMed ID: 8406476
    [Abstract] [Full Text] [Related]

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