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Journal Abstract Search

169 related items for PubMed ID: 9063701

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  • 2. 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; 10(1):38-44. PubMed ID: 7691111
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  • 5. 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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  • 6. [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 13; 29(11):1889-94. PubMed ID: 8307376
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  • 11. Human C7 polymorphism: classification and association analysis with C6.
    Washio K, Tokunaga K, Omoto K, Misawa S.
    Jinrui Idengaku Zasshi; 1986 Dec 13; 31(4):345-52. PubMed ID: 3613240
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  • 14. 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 13; 89(3):485-9. PubMed ID: 1516263
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  • 15. 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 Sep 13; 44(4):270-1. PubMed ID: 10429371
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  • 16. 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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