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269 related items for PubMed ID: 7762578

  • 1. Genetic detection of the silent allele (*Q0) in hereditary deficiencies of the human complement C6, C7, and C9 components.
    Alvarez V, Coto E, Setién F, Spath PJ, López-Larrea C.
    Am J Med Genet; 1995 Feb 13; 55(4):408-13. PubMed ID: 7762578
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  • 3. Three Japanese families with members carrying C7 silent allele (C7*Q0). Possibility for an association between C7*Q0 and C6*B.
    Nishimukai H, Kitamura H, Takeuchi Y, Shinomiya T, Tamaki Y.
    Hum Hered; 1988 Feb 13; 38(4):246-50. PubMed ID: 3169800
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  • 4. The human complement C9 gene: identification of two mutations causing deficiency and revision of the gene structure.
    Witzel-Schlömp K, Späth PJ, Hobart MJ, Fernie BA, Rittner C, Kaufmann T, Schneider PM.
    J Immunol; 1997 May 15; 158(10):5043-9. PubMed ID: 9144525
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  • 5. DNA polymorphisms and linkage relationship of the human complement component C6, C7, and C9 genes.
    Coto E, Martínez-Naves E, Domínguez O, DiScipio RG, Urra JM, López-Larrea C.
    Immunogenetics; 1991 May 15; 33(3):184-7. PubMed ID: 1672663
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  • 6. Reference typing report for complement components C6, C7 and C9 including mutations leading to deficiencies.
    Würzner R, Witzel-Schlömp K, Tokunaga K, Fernie BA, Hobart MJ, Orren A.
    Exp Clin Immunogenet; 1998 May 15; 15(4):268-85. PubMed ID: 10072638
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  • 7. Association of a 12.5-kilobase allele of the MspI restriction fragment length polymorphism of the C6 gene in patients with total deficiency of the sixth component of complement.
    Potter PC, Warburton C, Würzner R, Orren A, Di Scipio R.
    Exp Clin Immunogenet; 1993 May 15; 10(1):38-44. PubMed ID: 7691111
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  • 9. Combined genetic deficiency of C6 and C7 in man.
    Lachmann PJ, Hobart MJ, Woo P.
    Clin Exp Immunol; 1978 Aug 15; 33(2):193-203. PubMed ID: 102474
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  • 12. C7 M/N protein polymorphism typing applied to inherited deficiencies of human complement proteins C6 and C7.
    Würzner R, Rance N, Potter PC, Hendricks ML, Lachmann PJ, Orren A.
    Clin Exp Immunol; 1992 Sep 15; 89(3):485-9. PubMed ID: 1516263
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  • 13. [Genetic polymorphism of the sixth (C6) and seventh (C7) components of complement in Russian rural inhabitants of the Tomsk region].
    Kucher AN, Puzyrev VP, Ivanova OF, Khu TsIu, Siuĭ TsTs, Du ZhF.
    Genetika; 1993 Nov 15; 29(11):1889-94. PubMed ID: 8307376
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  • 14. A physical map of the human complement component C6, C7, and C9 genes.
    Setién F, Alvarez V, Coto E, DiScipio RG, López-Larrea C.
    Immunogenetics; 1993 Nov 15; 38(5):341-4. PubMed ID: 8344719
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  • 15. C7 deficiency in an Irish family: a deletion defect which is predominant in the Irish.
    O'Hara AM, Fernie BA, Moran AP, Williams YE, Connaughton JJ, Orren A, Hobart MJ.
    Clin Exp Immunol; 1998 Dec 15; 114(3):355-61. PubMed ID: 9844043
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  • 16. An NcoI polymorphism in the human complement component 7 (C7) gene.
    Horiuchi T, Nishizaka H, Tsukamoto H, Harashima S, Sawabe T, Morita C, Niho Y.
    J Hum Genet; 1999 Dec 15; 44(4):270-1. PubMed ID: 10429371
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  • 17. Complement C6 and C7 DNA polymorphisms analysed by PCR in seven ethnic groups and characterisation of the C6 MspI RFLP.
    Fernie BA, Finlay A, Price D, Chan E, Orren A, Joysey VC, Joysey KA, Hobart MJ.
    Exp Clin Immunogenet; 1996 Dec 15; 13(2):92-103. PubMed ID: 9063701
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  • 18. DNA polymorphism of the human complement component C7 gene in familial deficiencies.
    Coto E, Martínez-Naves E, Domínguez O, López-Larrea C.
    Hum Genet; 1990 Jul 15; 85(2):251-2. PubMed ID: 1973405
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  • 19. The role of complement in anti-bacterial defence.
    D'Amelio R, Biselli R.
    Ann Ital Med Int; 1994 Jul 15; 9(3):173-7. PubMed ID: 7946895
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  • 20. Heterogeneity in the genetic basis of human complement C9 deficiency.
    Witzel-Schlömp K, Hobart MJ, Fernie BA, Orren A, Würzner R, Rittner C, Kaufmann T, Schneider PM.
    Immunogenetics; 1998 Jul 15; 48(2):144-7. PubMed ID: 9634479
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