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3. Linkage relationship of C2 deficiency, HLA and glyoxalase I loci. Mahowald ML; Dalmasso AP; Petzel RA; Yunis EJ Vox Sang; 1979; 37(6):321-8. PubMed ID: 161677 [TBL] [Abstract][Full Text] [Related]
4. The chromosomal order of genes controlling the major histocompatibility complex, properdin factor B, and deficiency of the second component of complement. Raum D; Glass D; Carpenter CB; Alper CA; Schur PH J Clin Invest; 1976 Nov; 58(5):1240-8. PubMed ID: 993342 [TBL] [Abstract][Full Text] [Related]
5. HLA antigen studies in a family with C2 deficiency. Opelz G; Glovsky MM J Immunogenet; 1976 Oct; 3(5):303-6. PubMed ID: 137935 [TBL] [Abstract][Full Text] [Related]
6. Hereditary C2 deficiency: Genetic studies and association with the HL-A system. Day NK; L'Esperance R; Good RA; Michael AF; Hansen JA; Dupont B; Jersild C J Exp Med; 1975 Jun; 141(6):1464-9. PubMed ID: 1127385 [TBL] [Abstract][Full Text] [Related]
11. Studies on the C2-deficiency gene in man. Mortensen JP; Buskjaer L; Lamm LU Immunology; 1980 Apr; 39(4):541-9. PubMed ID: 7380478 [TBL] [Abstract][Full Text] [Related]
12. Linkage of gene for C2 deficiency and the major histocompatibility complex MHC in man. Family study of a further case. Day NK; Rubinstein P; Case D; Hansen JA; Good RA; Walker ME; Tulchin N; Dupont B; Jersild C Vox Sang; 1976; 31(2):96-102. PubMed ID: 133535 [TBL] [Abstract][Full Text] [Related]
13. Mixed lymphocyte culture determinants and C2 deficiency: LD-7a associated with C2 deficiency in four families. Fu SM; Stern R; Kunkel HG; Dupont B; Hansen JA; Day NK; Good RA; Jersild C; Fotino M J Exp Med; 1975 Aug; 142(2):495-506. PubMed ID: 124762 [TBL] [Abstract][Full Text] [Related]
14. Deficiency of C2, the second complement component, in the family of a patient with SLE-like syndrome: the first case of hereditary C2 deficiency in Czechoslovakia. Starsia Z; Zitnan D; Loos M; Stefanovic J; Bosák V; Niks M; Tomanová H; Lukác J; Lulovicová M Haematologia (Budap); 1987; 20(4):215-20. PubMed ID: 3428724 [TBL] [Abstract][Full Text] [Related]
16. Selective deficiencies in complement component : a family with hereditary C2 deficiency. Dantant M; Rivat C; Gilbert D; Fontaine M; Cavelier B; Godin M; Fillastre JP Biomedicine; 1978; 28(3):185-90. PubMed ID: 698338 [TBL] [Abstract][Full Text] [Related]
17. HLA genotypes in a family with a case of homozygous C2 deficiency and discoid lupus erythematosus. Braathen LR; Bratlie A; Teisberg P Acta Derm Venereol; 1986; 66(5):419-22. PubMed ID: 2431580 [TBL] [Abstract][Full Text] [Related]
18. Characterization of type I complement C2 deficiency MHC haplotypes. Strong conservation of the complotype/HLA-B-region and absence of disease association due to linked class II genes. Truedsson L; Alper CA; Awdeh ZL; Johansen P; Sjöholm AG; Sturfelt G J Immunol; 1993 Nov; 151(10):5856-63. PubMed ID: 7901282 [TBL] [Abstract][Full Text] [Related]
19. Association of the C2-deficiency gene (C2*QO) with the C4A*4, C4B*2 genes. Hauptmann G; Tongio MM; Goetz J; Mayer S; Fauchet R; Sobel A; Griscel C; Berthoux F; Rivat C; Rother U J Immunogenet; 1982 Apr; 9(2):127-32. PubMed ID: 7086154 [No Abstract] [Full Text] [Related]
20. Renal transplantation in a patient with hereditary deficiency of the second component of complement. Zeitz HJ; Gewurz A; Jonasson O; Geis WP; Gewurz H Clin Exp Immunol; 1981 Nov; 46(2):420-4. PubMed ID: 7039890 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]