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Journal Abstract Search

180 related items for PubMed ID: 6980755

  • 1. Complement C4 allotypes in congenital adrenal hyperplasia due to 21-hydroxylase deficiency: further evidence for different allelic variants at the 21-hydroxylase locus.
    O'Neill GJ, Dupont B, Pollack MS, Levine LS, New MI.
    Clin Immunol Immunopathol; 1982 May; 23(2):312-22. PubMed ID: 6980755
    [No Abstract] [Full Text] [Related]

  • 2. Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants.
    Schneider PM, Carroll MC, Alper CA, Rittner C, Whitehead AS, Yunis EJ, Colten HR.
    J Clin Invest; 1986 Sep; 78(3):650-7. PubMed ID: 3018042
    [Abstract] [Full Text] [Related]

  • 3. Gene conversion in salt-losing congenital adrenal hyperplasia with absent complement C4B protein.
    Donohoue PA, van Dop C, McLean RH, White PC, Jospe N, Migeon CJ.
    J Clin Endocrinol Metab; 1986 May; 62(5):995-1002. PubMed ID: 3007562
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  • 4. Deletion of the steroid 21-hydroxylase and complement C4 genes in congenital adrenal hyperplasia.
    Rumsby G, Carroll MC, Porter RR, Grant DB, Hjelm M.
    J Med Genet; 1986 Jun; 23(3):204-9. PubMed ID: 3487654
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  • 5. 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; 26(1):10-7. PubMed ID: 2783976
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  • 6. Steroid 21-hydroxylase deficiency and the major histocompatibility complex.
    White PC, Werkmeister J, New MI, Dupont B.
    Hum Immunol; 1986 Apr; 15(4):404-15. PubMed ID: 3009365
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  • 7. 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; 1(1):55-66. PubMed ID: 6266983
    [No Abstract] [Full Text] [Related]

  • 8. 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 Jul; 458():36-40. PubMed ID: 3879128
    [No Abstract] [Full Text] [Related]

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  • 11. Major-histocompatibility-complex gene markers and restriction-fragment analysis of steroid 21-hydroxylase (CYP21) and complement C4 genes in classical congenital adrenal hyperplasia patients in a single population.
    Partanen J, Koskimies S, Sipilä I, Lipsanen V.
    Am J Hum Genet; 1989 May; 44(5):660-70. PubMed ID: 2565078
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  • 12. [Connection between congenital adrenal hyperplasia due to 21-hydroxylase deficiency and the HLA genotype].
    Dumić M, Brkljacić L, Krzisnik C, Radica A, Tajić M, Kastelan A.
    Lijec Vjesn; 1983 May; 105(7-8):290-2. PubMed ID: 6605467
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  • 14. 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
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  • 15. [Genetic of the 21 hydroxylase deficiency].
    Boué A, Couillin P, Pomarède R, Rappaport R, Boué J.
    Ann Endocrinol (Paris); 1982 Apr 02; 43(1):3-14. PubMed ID: 6982657
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  • 16. Molecular cloning of steroid 21-hydroxylase.
    White PC, Dupont B, New MI.
    Endocr Res; 1982 Apr 02; 10(3-4):335-45. PubMed ID: 6336060
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  • 19. 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 Apr 02; 25(2):99-103. PubMed ID: 3493216
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