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Journal Abstract Search

287 related items for PubMed ID: 7691111

  • 21. Properties of a low molecular weight complement component C6 found in human subjects with subtotal C6 deficiency.
    Orren A, Würzner R, Potter PC, Fernie BA, Coetzee S, Morgan BP, Lachmann PJ.
    Immunology; 1992 Jan; 75(1):10-6. PubMed ID: 1537585
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  • 22. Incomplete functional deficiencies of the fourth (C4) and second (C2) components of complement in a patient with linear frontoparietal scleroderma and his family. Deficiencies determined by a gene not linked to human leukocyte antigen system.
    Venneker GT, van Meegen M, de Kok-Nazaruk M, Hulsmans RF, de Waall LP, Bos JD, Asghar SS.
    Exp Clin Immunogenet; 1996 Jan; 13(2):104-11. PubMed ID: 9063702
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  • 25. 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 Jan; 33(3):184-7. PubMed ID: 1672663
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  • 27. Association between a 10 kb Pvu II restriction fragment of genomic DNA with the hemochromatosis gene.
    Lucotte G, Coulondre C.
    Exp Clin Immunogenet; 1986 Jan; 3(4):219-23. PubMed ID: 2908538
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  • 28. Combined hereditary deficiency of the sixth component of complement and factor VIII coagulant activity in a Dutch family.
    Daha MR, Bertina RM, Thompson J, Kauffmann RH, Nicholson-Weller A, Veltkamp JJ, Briët E.
    Clin Exp Immunol; 1982 Jun; 48(3):733-8. PubMed ID: 6811172
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  • 30. Familial late complement component (C6, C7) deficiency with chronic meningococcemia.
    Clough JD, Clough ML, Weinstein A, Calabrese LH, Mansfield LR, Gulick P, Gavan T, Braun WE.
    Arch Intern Med; 1980 Jul; 140(7):929-33. PubMed ID: 7387302
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  • 35. Restrictive fragment length polymorphisms of markers 3'HVR and 24-1 and their applications in gene diagnosis of adult polycystic disease in Chinese.
    Zhang SZ, Ding L, Yu YL, Hu Y, Luo NF, Zhang SX, Li H.
    Chin Med J (Engl); 1994 Jan; 107(1):47-52. PubMed ID: 7910547
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  • 36. A DNA restriction fragment length polymorphism in the complement region of the human MHC shows an absolute correlation with polymorphism of complement factor B(Bf) defined by isoelectric focusing.
    Fathallah D, Abbal M, Thomsen M, Cambon-Thomsen A, Campbell RD.
    J Immunogenet; 1985 Dec; 12(6):321-6. PubMed ID: 3016098
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  • 39. 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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