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Journal Abstract Search
175 related items for PubMed ID: 6130199
21. Major-histocompatibility-complex extended haplotypes in membranoproliferative glomerulonephritis. Welch TR, Beischel L, Balakrishnan K, Quinlan M, West CD. N Engl J Med; 1986 Jun 05; 314(23):1476-81. PubMed ID: 3458025 [Abstract] [Full Text] [Related]
22. Comparison of the structure of HLA-Bw47 to HLA-B13 and its relationship to 21-hydroxylase deficiency. Zemmour J, Ennis PD, Parham P, Dupont B. Immunogenetics; 1988 Jun 05; 27(4):281-7. PubMed ID: 3257938 [Abstract] [Full Text] [Related]
23. 21-hydroxylase deficiency families with HLA identical affected and unaffected sibs. Sinnott PJ, Dyer PA, Price DA, Harris R, Strachan T. J Med Genet; 1989 Jan 05; 26(1):10-7. PubMed ID: 2783976 [Abstract] [Full Text] [Related]
24. Heterozygotes and cryptic patients in families of patients with congenital adrenal hyperplasia (21-hydroxylase deficiency). HLA and glyoxalase I typing and hormonal studies. Petersen KE, Svejgaard A, Nielsen MD, Dissing J. Horm Res; 1982 Jan 05; 16(3):151-9. PubMed ID: 6286442 [Abstract] [Full Text] [Related]
25. HLA-A, B, C, DR alleles in congenital adrenal hyperplasia. Couillin P, Kottler-Missonnier ML, Grisard MC, Hors J, Feingold J, Boué J, Boué A. Hum Genet; 1980 Jan 05; 53(3):389-92. PubMed ID: 6966250 [Abstract] [Full Text] [Related]
26. Extended major histocompatibility complex haplotypes in type I diabetes mellitus. Raum D, Awdeh Z, Yunis EJ, Alper CA, Gabbay KH. J Clin Invest; 1984 Aug 05; 74(2):449-54. PubMed ID: 6746903 [Abstract] [Full Text] [Related]
27. Hormonal profiles in Italian late-onset adrenal hyperplasia correlate with HLA class III polymorphisms. Balsamo A, Revelli A, Borelli I, Amoroso A, Cenderelli G, De Sanso G, Mazzola G, Curtoni ES, Zoppetti G, Massobrio M. Gynecol Endocrinol; 1992 Jun 05; 6(2):91-8. PubMed ID: 1354409 [Abstract] [Full Text] [Related]
28. Molecular heterogeneity of second and fourth components of complement and their genes in systemic sclerosis and association of HLA alleles A1, B8 and DR3 with limited and DR5 with diffuse systemic sclerosis. Venneker GT, van den Hoogen FH, van Meegen M, de Kok-Nazaruk M, Hulsmans RF, Boerbooms AM, de Waal LP, Bos JD, Asghar SS. Exp Clin Immunogenet; 1998 Jun 05; 15(2):90-9. PubMed ID: 9691203 [Abstract] [Full Text] [Related]
29. A haplotype study of HLA complex with special reference to the HLA-DR series and to Bf. C2 and glyoxalase I polymorphisms. Dausset J, Legrand L, Lepage V, Contu L, Marcelli-Barge A, Wildloecher I, Benajam A, Meo T, Degos L. Tissue Antigens; 1978 Oct 05; 12(4):297-307. PubMed ID: 83027 [Abstract] [Full Text] [Related]
30. Extended MHC haplotypes in salt-losing 21-hydroxylase deficiency. Alper CA, Fleischnick E, Awdeh Z, Raum D, Crigler JF, Gerald PS, Yunis EJ. Ann N Y Acad Sci; 1985 Oct 05; 458():28-35. PubMed ID: 3879127 [No Abstract] [Full Text] [Related]
31. Molecular heterogeneity of the fourth component of complement (C4) and its genes in vitiligo. Venneker GT, Westerhof W, de Vries IJ, Drayer NM, Wolthers BG, de Waal LP, Bos JD, Asghar SS. J Invest Dermatol; 1992 Dec 05; 99(6):853-8. PubMed ID: 1469300 [Abstract] [Full Text] [Related]
32. An approach to mapping haplotype-specific recombination sites in human MHC class III. Levo A, Westman P, Partanen J. Immunogenetics; 1996 Dec 05; 43(3):136-40. PubMed ID: 8550097 [Abstract] [Full Text] [Related]
33. The effect of ethnicity on major histocompatibility complex complement allotypes and extended haplotypes in patients with systemic lupus erythematosus. Schur PH, Marcus-Bagley D, Awdeh Z, Yunis EJ, Alper CA. Arthritis Rheum; 1990 Jul 05; 33(7):985-92. PubMed ID: 2369433 [Abstract] [Full Text] [Related]
34. Unrelated individuals matched for MHC extended haplotypes and HLA-identical siblings show comparable responses in mixed lymphocyte culture. Awdeh ZL, Alper CA, Eynon E, Alosco SM, Stein R, Yunis EJ. Lancet; 1985 Oct 19; 2(8460):853-6. PubMed ID: 2864576 [Abstract] [Full Text] [Related]
35. [HLA antigens and different clinical forms of 21-hydroxylase deficiency in the French population]. Couillin P, Ravisé N, Hors J, Feingold J, Rappaport R, Kuttenn F, Boué A. Pathol Biol (Paris); 1986 Jun 19; 34(6):789-94. PubMed ID: 3531997 [Abstract] [Full Text] [Related]
36. The MHC in human bone marrow allotransplantation. Yunis EJ, Awdeh Z, Raum D, Alper CA. Clin Haematol; 1983 Oct 19; 12(3):641-80. PubMed ID: 6227438 [Abstract] [Full Text] [Related]
37. Identification of HLA-B44 subtypes associated with extended MHC haplotypes. Kruskall MS, Eynon EE, Awdeh Z, Alper CA, Yunis EJ. Immunogenetics; 1987 Oct 19; 26(4-5):216-9. PubMed ID: 3653939 [Abstract] [Full Text] [Related]
38. An unusual "morphologic" variant of BF S. Raum D, Surgenor T, Awdeh Z, Marcus D, Blumenthal M, Yunis EJ, Alper CA. Am J Hum Genet; 1984 Mar 19; 36(2):346-51. PubMed ID: 6585138 [Abstract] [Full Text] [Related]
39. HLA class III haplotypes in multicase rheumatoid arthritis families. Fielder AH, Ollier W, Lord DK, Burley MW, Silman A, Awad J, Festenstein H, Batchelor JR. Hum Immunol; 1989 Jun 19; 25(2):75-85. PubMed ID: 2737929 [Abstract] [Full Text] [Related]
40. [HLA haplotypes in families of children with congenital adrenal hyperplasia]. Turowska-Heydel D, Pietrzyk JJ, Turowski G. Pediatr Pol; 1995 Feb 19; 70(2):115-20. PubMed ID: 7603793 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]