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Journal Abstract Search

143 related items for PubMed ID: 2892683

  • 1. Early diagnosis in X-linked agammaglobulinaemia.
    Schuurman RK, Mensink EJ, Sandkuyl LA, Post ED, van Velzen-Blad H.
    Eur J Pediatr; 1988 Jan; 147(1):93-5. PubMed ID: 2892683
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  • 2. 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
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  • 3. 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
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  • 4. 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
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  • 7. A new restriction fragment length polymorphism at the DXS101 locus allows carrier detection in a family with X linked agammaglobulinaemia.
    Sweatman A, Lovering R, Middleton-Price H, Jones A, Morgan G, Levinsky R, Kinnon C.
    J Med Genet; 1993 Jun; 30(6):512-4. PubMed ID: 8100857
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  • 8. 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
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  • 9. 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
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  • 10. Carrier detection in typical and atypical X-linked agammaglobulinemia.
    Conley ME, Puck JM.
    J Pediatr; 1988 May; 112(5):688-94. PubMed ID: 2896233
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  • 11. 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
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  • 12. 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
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  • 13. X-linked agammaglobulinemia.
    Timmers E, de Weers M, Alt FW, Hendriks RW, Schuurman RK.
    Clin Immunol Immunopathol; 1991 Nov; 61(2 Pt 2):S83-93. PubMed ID: 1934617
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  • 14. Deletion within the Src homology domain 3 of Bruton's tyrosine kinase resulting in X-linked agammaglobulinemia (XLA).
    Zhu Q, Zhang M, Rawlings DJ, Vihinen M, Hagemann T, Saffran DC, Kwan SP, Nilsson L, Smith CI, Witte ON, Chen SH, Ochs HD.
    J Exp Med; 1994 Aug 01; 180(2):461-70. PubMed ID: 7519238
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  • 15. X linked agammaglobulinaemia with a 'leaky' phenotype.
    Jones A, Bradley L, Alterman L, Tarlow M, Thompson R, Kinnon C, Morgan G.
    Arch Dis Child; 1996 Jun 01; 74(6):548-9. PubMed ID: 8758136
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  • 16. Carrier detection and prenatal diagnosis of X-linked agammaglobulinemia.
    Journet O, Durandy A, Doussau M, Le Deist F, Couvreur J, Griscelli C, Fischer A, de Saint-Basile G.
    Am J Med Genet; 1992 Jul 15; 43(5):885-7. PubMed ID: 1642281
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  • 17. Molecular analysis of X-linked agammaglobulinemia with growth hormone deficiency.
    Conley ME, Burks AW, Herrod HG, Puck JM.
    J Pediatr; 1991 Sep 15; 119(3):392-7. PubMed ID: 1880652
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  • 18. 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 15; 73(4):327-32. PubMed ID: 3502688
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