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Journal Abstract Search

120 related items for PubMed ID: 6266985

  • 1. Intra-HLA recombinations localizing the 21-hydroxylase deficiency gene within the HLA complex.
    Bias WB, Urban MD, Migeon CJ, Hsu SH, Lee PA.
    Hum Immunol; 1981 Mar; 2(2):139-45. PubMed ID: 6266985
    [Abstract] [Full Text] [Related]

  • 2. HLA typing and ACTH stimulation in the detection of carriers for 21-hydroxylase deficiency.
    Stuckey MS, Boyne P, Macdonald WB, Christiansen FT, Houliston JB, Dawkins RL.
    Aust N Z J Med; 1980 Oct; 10(5):552-4. PubMed ID: 6258552
    [Abstract] [Full Text] [Related]

  • 3. 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 Oct; 16(3):151-9. PubMed ID: 6286442
    [Abstract] [Full Text] [Related]

  • 4. Sharing of MHC haplotypes among apparently unrelated patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Layrisse Z, White C, Gunczler P, Gafaro Valera L, Arias S, Yunis EJ, Alper CA, Awdeh ZL.
    Immunogenetics; 1987 Oct; 25(2):99-103. PubMed ID: 3493216
    [Abstract] [Full Text] [Related]

  • 5. Complotype genetic loci segregate more frequently with HLA-DR than with HLA-B.
    Yunis EJ, Awdeh Z, Johnson A, Suciu-Foca N, Robinson MA, Hartzman R, Raum D, Fleischnick E, Alper CA.
    Immunogenetics; 1985 Oct; 21(1):25-31. PubMed ID: 3871424
    [Abstract] [Full Text] [Related]

  • 6. Late-onset form of congenital adrenal hyperplasia in the HLA-B14; DR1 haplotype is caused by a duplication in the 21-OH MHC gene region.
    Boehm BO, Rosak C, Kuehnl P, Schöffling K.
    Horm Metab Res; 1986 Nov; 18(11):791-2. PubMed ID: 3491779
    [No Abstract] [Full Text] [Related]

  • 7. Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1.
    Speiser PW, New MI, White PC.
    N Engl J Med; 1988 Jul 07; 319(1):19-23. PubMed ID: 3260007
    [Abstract] [Full Text] [Related]

  • 8. 21-Hydroxylase deficiency: HLA genotypes and hormonal phenotypes in the families of 32 Italian patients.
    Livieri C, Belvedere M, Martinetti M, Beluffi G, Fiori P, Cogliati CR, Goffredo V, Lorini R, Severi F.
    Prog Clin Biol Res; 1985 Jul 07; 200():243-55. PubMed ID: 3001775
    [No Abstract] [Full Text] [Related]

  • 9. Anomalous mixed lymphocyte culture reactivity between HLA--A, --B, --C, --DR identical siblings.
    Reinsmoen NL, Noreen HJ, Friend PS, Giblett ER, Greenberg LJ, Kersey JH.
    Tissue Antigens; 1979 Jan 07; 13(1):19-34. PubMed ID: 154195
    [Abstract] [Full Text] [Related]

  • 10. The attenuated form of congenital adrenal hyperplasia as an allelic form of 21-hydroxylase deficiency.
    Migeon CJ, Rosenwaks Z, Lee PA, Urban MD, Bias WB.
    J Clin Endocrinol Metab; 1980 Sep 07; 51(3):647-9. PubMed ID: 6251108
    [Abstract] [Full Text] [Related]

  • 11. [Genetic of the 21 hydroxylase deficiency].
    Boué A, Couillin P, Pomarède R, Rappaport R, Boué J.
    Ann Endocrinol (Paris); 1982 Sep 07; 43(1):3-14. PubMed ID: 6982657
    [Abstract] [Full Text] [Related]

  • 12. Defective antigen presentation and novel structural properties of DR1 from an HLA haplotype associated with 21-hydroxylase deficiency.
    Davis JE, Rich RR, Van M, Le HV, Pollack MS, Cook RG.
    J Clin Invest; 1987 Oct 07; 80(4):998-1008. PubMed ID: 2443540
    [Abstract] [Full Text] [Related]

  • 13. Basic and clinical aspects of congenital adrenal hyperplasia.
    New MI.
    J Steroid Biochem; 1987 Oct 07; 27(1-3):1-7. PubMed ID: 3320531
    [Abstract] [Full Text] [Related]

  • 14. The HLA associations in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a Yugoslav population.
    Kastelan A, Brkljacić-Surkalović L, Dumić M.
    Ann N Y Acad Sci; 1985 Oct 07; 458():36-40. PubMed ID: 3879128
    [No Abstract] [Full Text] [Related]

  • 15. Genetics and biochemical variability of variants of 21 hydroxylase deficiency.
    Gordon MT, Conway DI, Anderson DC, Harris R.
    J Med Genet; 1985 Oct 07; 22(5):354-60. PubMed ID: 3001309
    [Abstract] [Full Text] [Related]

  • 16. The coexistence of IgA deficiency and 21-hydroxylase deficiency marked by specific MHC supratypes.
    Cobain TJ, Stuckey MS, McCluskey J, Wilton AN, Gedeon A, Garlepp MJ, Christiansen FT, Dawkins RL.
    Ann N Y Acad Sci; 1985 Oct 07; 458():76-84. PubMed ID: 3879134
    [No Abstract] [Full Text] [Related]

  • 17. MHC "supratype" predicting heterozygous 21-hydroxylase deficiency.
    McCluskey J, Kay PH, Stuckey M, Christiansen FT, Dawkins RL, Wilson G.
    Lancet; 1983 Apr 02; 1(8327):764-5. PubMed ID: 6132105
    [No Abstract] [Full Text] [Related]

  • 18. [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 02; 34(6):789-94. PubMed ID: 3531997
    [Abstract] [Full Text] [Related]

  • 19. Late onset 21-hydroxylase deficiency and HLA in the Ashkenazi population: a new allele at the 21-hydroxylase locus.
    Laron Z, Pollack MS, Zamir R, Roitman A, Dickerman Z, Levine LS, Lorenzen F, O'Neill GJ, Pang S, New MI, Dupont B.
    Hum Immunol; 1980 Jul 02; 1(1):55-66. PubMed ID: 6266983
    [No Abstract] [Full Text] [Related]

  • 20. Attenuated forms of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
    Lee PA, Rosenwaks Z, Urban MD, Migeon CJ, Bias WD.
    J Clin Endocrinol Metab; 1982 Nov 02; 55(5):866-71. PubMed ID: 6288754
    [Abstract] [Full Text] [Related]

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