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The Journal of Rheumatology|August 1, 1983
Selective complete Clq deficiency associated with systemic lupus erythematosusK Steinsson, R H McLean, M Merrow, et al.Pediatric Nephrology (Berlin, Germany)|November 1, 1990
Recurrent haemolytic uraemic syndrome and acquired hypomorphic variant of the third component of complementA M Roodhooft, R H McLean, E Elst, et al.Journal of Immunology (Baltimore, Md. : 1950)|November 1, 1979
Preservation of C3, C5, and C5a functional activities by a new radiolabeling method; demonstration of C5 products in complement-activated serumD L Kreutzer, S Kunkel, P A Ward, et al.FEBS Letters|January 29, 1990
Hypomorphic C4B* 15 variant of the fourth component of complementM J Christenson, T LaRosa, M Jung, et al.Arthritis and Rheumatism|June 1, 1988
Molecular heterogeneity of complement component C4-null and 21-hydroxylase genes in systemic lupus erythematosusR Goldstein, F C Arnett, R H McLean, et al.The Journal of Clinical Investigation|October 1, 1992
A unique recombination event resulting in a C4A*Q0,C4B*Q0 double null haplotypeM B Fasano, J A Winkelstein, T LaRosa, et al.Journal of Clinical Immunology|April 1, 1982
Partial H (beta 1H) deficiency and glomerulonephritis in two familiesR J Wyatt, B A Julian, A Weinstein, et al.Tissue Antigens|February 1, 1990
Characterization of two hybrid C4 allotypes (C4A*12 and C4B*3) by electrophoretic, serological and restriction fragment length polymorphism analysesR H McLean, W B Bias, C Giles, et al.The Journal of Pediatrics|February 1, 1982
Serum hemolytic factor D values in children with steroid-responsive idiopathic nephrotic syndromeM Ballow, T L Kennedy, K M Gaudio, et al.The American Journal of Medicine|August 1, 1986
Relationship between C4 null genes, HLA-D region antigens, and genetic susceptibility to systemic lupus erythematosus in Caucasian and black AmericansP F Howard, M C Hochberg, W B Bias, et al.Pageof 21