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Journal Abstract Search

191 related items for PubMed ID: 2888720

  • 1. 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; 77(2):172-4. PubMed ID: 2888720
    [Abstract] [Full Text] [Related]

  • 2. Close linkage of probe p212 (DXS178) to X-linked agammaglobulinemia.
    Guioli S, Arveiler B, Bardoni B, Notarangelo LD, Panina P, Duse M, Ugazio A, Oberlé I, de Saint Basile G, Mandel JL.
    Hum Genet; 1989 Dec; 84(1):19-21. PubMed ID: 2575070
    [Abstract] [Full Text] [Related]

  • 3. 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
    [Abstract] [Full Text] [Related]

  • 4. 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
    [Abstract] [Full Text] [Related]

  • 5. Genetic prediction in X-linked agammaglobulinaemia.
    Lau YL, Levinsky RJ, Malcolm S, Goodship J, Winter R, Pembrey M.
    Am J Med Genet; 1988 Oct; 31(2):437-48. PubMed ID: 3232706
    [Abstract] [Full Text] [Related]

  • 6. Genetic heterogeneity in X-linked agammaglobulinemia complicates carrier detection and prenatal diagnosis.
    Mensink EJ, Thompson A, Schot JD, Kraakman ME, Sandkuyl LA, Schuurman RK.
    Clin Genet; 1987 Feb; 31(2):91-6. PubMed ID: 2881637
    [Abstract] [Full Text] [Related]

  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Mapping of a gene for X-linked agammaglobulinemia and evidence for genetic heterogeneity.
    Mensink EJ, Thompson A, Schot JD, van de Greef WM, Sandkuyl LA, Schuurman RK.
    Hum Genet; 1986 Aug; 73(4):327-32. PubMed ID: 3502688
    [Abstract] [Full Text] [Related]

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  • 11. Heterogeneity in the map distance between X-linked agammaglobulinemia and a map of nine RFLP loci.
    Ott J, Mensink EJ, Thompson A, Schot JD, Schuurman RK.
    Hum Genet; 1986 Nov; 74(3):280-3. PubMed ID: 2877937
    [Abstract] [Full Text] [Related]

  • 12. Multipoint linkage analysis in X-linked Alport syndrome.
    Hertz JM, Kruse TA, Thomsen A, Spencer ES.
    Hum Genet; 1991 Dec; 88(2):157-61. PubMed ID: 1684562
    [Abstract] [Full Text] [Related]

  • 13. Genetic mapping of two loci, DXS454 and DXS458, with respect to the X-linked agammaglobulinemia gene locus.
    Parkar M, Lovering R, Levinsky RJ, Kinnon C.
    Hum Genet; 1994 Jan; 93(1):89-90. PubMed ID: 8270264
    [Abstract] [Full Text] [Related]

  • 14. Isolation and mapping of discrete DXS101 loci in Xq22 near the X-linked agammaglobulinaemia gene locus.
    O'Reilly MA, Sweatman AK, Bradley LD, Alterman LA, Lovering R, Malcolm S, Levinsky RJ, Kinnon C.
    Hum Genet; 1993 Jul; 91(6):605-8. PubMed ID: 8101833
    [Abstract] [Full Text] [Related]

  • 15. Molecular analysis of X-linked agammaglobulinemia with growth hormone deficiency.
    Conley ME, Burks AW, Herrod HG, Puck JM.
    J Pediatr; 1991 Sep; 119(3):392-7. PubMed ID: 1880652
    [Abstract] [Full Text] [Related]

  • 16. Identification of CpG islands around the DXS178 locus in the region of the X-linked agammaglobulinaemia gene locus in Xq22.
    O'Reilly MA, Alterman LA, Malcolm S, Levinsky RJ, Kinnon C.
    Hum Genet; 1992 Nov; 90(3):275-8. PubMed ID: 1487242
    [Abstract] [Full Text] [Related]

  • 17. A new RFLP marker, SP282, at the btk locus for genetic analysis in X-linked agammaglobulinaemia families.
    Kwan SP, Walker AP, Hagemann T, Gupta S, Vayuvegula B, Ochs HD.
    Prenat Diagn; 1994 Jun; 14(6):493-6. PubMed ID: 7937587
    [Abstract] [Full Text] [Related]

  • 18. Evidence for male X chromosomal mosaicism in X-linked agammaglobulinemia.
    Hendriks RW, Mensink EJ, Kraakman ME, Thompson A, Schuurman RK.
    Hum Genet; 1989 Oct; 83(3):267-70. PubMed ID: 2571563
    [Abstract] [Full Text] [Related]

  • 19. 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
    [Abstract] [Full Text] [Related]

  • 20. Identification of deletions in the btk gene allows unambiguous assessment of carrier status in families with X-linked agammaglobulinaemia.
    Lovering RC, Sweatman A, Genet SA, Middleton-Price HR, Vetrie D, Vorechovsky I, Bentley D, Fontan G, Español T, Morgan G.
    Hum Genet; 1994 Jul; 94(1):77-9. PubMed ID: 8034298
    [Abstract] [Full Text] [Related]

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