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Journal Abstract Search

174 related items for PubMed ID: 2878869

  • 1. Associations between restriction fragment length polymorphisms detected with a probe for human 21-hydroxylase (21-OH) and two clinical forms of 21-OH deficiency.
    Mornet E, Couillin P, Kutten F, Raux MC, White PC, Cohen D, Boué A, Dausset J.
    Hum Genet; 1986 Dec; 74(4):402-8. PubMed ID: 2878869
    [Abstract] [Full Text] [Related]

  • 2. HLA-linked congenital adrenal hyperplasia results from a defective gene encoding a cytochrome P-450 specific for steroid 21-hydroxylation.
    White PC, New MI, Dupont B.
    Proc Natl Acad Sci U S A; 1984 Dec; 81(23):7505-9. PubMed ID: 6334310
    [Abstract] [Full Text] [Related]

  • 3. Classical and late-onset forms of congenital adrenal hyperplasia caused by 21-OH deficiency reveal different alterations in the C4/21-OH gene region.
    Boehm BO, Rosak C, Boehm TL, Kuehnl P, White PC, Schöffling K.
    Mol Biol Med; 1986 Oct; 3(5):437-48. PubMed ID: 2882404
    [Abstract] [Full Text] [Related]

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

  • 5. 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
    [Abstract] [Full Text] [Related]

  • 6. Restriction maps and restriction fragment length polymorphisms of the human 21-hydroxylase genes.
    Donohoue PA, Jospe N, Migeon CJ, McLean RH, Bias WB, White PC, Van Dop C.
    Biochem Biophys Res Commun; 1986 Apr 29; 136(2):722-9. PubMed ID: 3010994
    [Abstract] [Full Text] [Related]

  • 7. Two genes encoding steroid 21-hydroxylase are located near the genes encoding the fourth component of complement in man.
    White PC, Grossberger D, Onufer BJ, Chaplin DD, New MI, Dupont B, Strominger JL.
    Proc Natl Acad Sci U S A; 1985 Feb 29; 82(4):1089-93. PubMed ID: 2983330
    [Abstract] [Full Text] [Related]

  • 8. 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 29; 44(5):660-70. PubMed ID: 2565078
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  • 10. Diagnosis of classical steroid 21-hydroxylase deficiency using an HLA-B locus-specific DNA-probe.
    Killeen AA, Seelig S, Ulstrom RA, Orr HT.
    Am J Med Genet; 1988 Mar 29; 29(3):703-12. PubMed ID: 2897792
    [Abstract] [Full Text] [Related]

  • 11. Steroid 21-hydroxylase deficiency and the major histocompatibility complex.
    White PC, Werkmeister J, New MI, Dupont B.
    Hum Immunol; 1986 Apr 29; 15(4):404-15. PubMed ID: 3009365
    [Abstract] [Full Text] [Related]

  • 12. First trimester prenatal diagnosis of 21-hydroxylase deficiency by linkage analysis to HLA-DNA probes and by 17-hydroxyprogesterone determination.
    Mornet E, Boue J, Raux-Demay M, Couillin P, Oury JF, Dumez Y, Dausset J, Cohen D, Boué A.
    Hum Genet; 1986 Aug 29; 73(4):358-64. PubMed ID: 3017844
    [Abstract] [Full Text] [Related]

  • 13. Molecular cloning of steroid 21-hydroxylase.
    White PC, Dupont B, New MI.
    Endocr Res; 1986 Aug 29; 10(3-4):335-45. PubMed ID: 6336060
    [Abstract] [Full Text] [Related]

  • 14. 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]

  • 15. Prenatal DNA analysis in four embryos/fetuses at risk of 21-hydroxylase deficiency.
    Matsumoto T, Kondoh T, Kamei T, Yoshimoto M, Tsuji Y, Suzumori K, Izumi R, Iwatani N, Niikawa N.
    Eur J Pediatr; 1988 Dec 07; 148(3):228-32. PubMed ID: 2905656
    [Abstract] [Full Text] [Related]

  • 16. Identification of a new HLA-B7-associated C21-hydroxylase deficiency gene by restriction enzyme length polymorphism.
    Keller E, Andreas-Zietz A, Knorr D, Scholz S, Albert ED.
    Immunogenetics; 1987 Dec 07; 25(2):123-5. PubMed ID: 2880800
    [No Abstract] [Full Text] [Related]

  • 17. 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 Dec 07; 25(2):99-103. PubMed ID: 3493216
    [Abstract] [Full Text] [Related]

  • 18. Heterogeneity of steroid 21-hydroxylase genes in classical congenital adrenal hyperplasia.
    Dawkins RL, Martin E, Kay PH, Garlepp MJ, Wilton AN, Stuckey MS.
    J Immunogenet; 1987 Dec 07; 14(2-3):89-98. PubMed ID: 2891769
    [Abstract] [Full Text] [Related]

  • 19. 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 07; 6(2):91-8. PubMed ID: 1354409
    [Abstract] [Full Text] [Related]

  • 20. HLA haplotypes and hormonal studies in 25 Italian families of patients with classical and non-classical 21-OH deficiency.
    Einaudi S, Borelli I, Lala R, Praticŏ L, Curtoni ES, De Sanctis C.
    J Pediatr Endocrinol; 1994 Jun 07; 7(4):349-55. PubMed ID: 7735374
    [Abstract] [Full Text] [Related]

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