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Journal Abstract Search

98 related items for PubMed ID: 8100857

  • 1. 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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  • 3. 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
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  • 4. Physical mapping identifies DXS265 as a useful genetic marker for carrier detection and prenatal diagnosis of X-linked agammaglobulinemia.
    Lovering R, Sweatman AK, O'Reilly MA, Genet SA, Middleton-Price H, Malcolm S, Levinsky RJ, Kinnon C.
    Hum Genet; 1993 Mar; 91(2):178-80. PubMed ID: 8462977
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  • 5. 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
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  • 6. 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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  • 8. 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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  • 9. 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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  • 10. 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]

  • 11. 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
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  • 13. 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
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  • 15. 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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  • 17. Carrier detection in agammaglobulinemia by X chromosome inactivation analysis.
    Miyashita T, Iwata T, Mizutani S, Kamoshita S, Kobayashi N.
    Acta Paediatr Jpn; 1992 Jun; 34(3):267-72. PubMed ID: 1354911
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  • 18. Application of carrier testing to genetic counseling for X-linked agammaglobulinemia.
    Allen RC, Nachtman RG, Rosenblatt HM, Belmont JW.
    Am J Hum Genet; 1994 Jan; 54(1):25-35. PubMed ID: 7506482
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  • 20. 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]

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