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Journal Abstract Search

116 related items for PubMed ID: 3531997

  • 1. [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; 34(6):789-94. PubMed ID: 3531997
    [Abstract] [Full Text] [Related]

  • 2. Different gene defects in the salt-wasting (SW), simple virilizing (SV), and nonclassical (NC) types of congenital adrenal hyperplasia (CAH).
    Knorr D, Albert ED, Bidlingmaier F, Höller W, Scholz S.
    Ann N Y Acad Sci; 1985 Jun; 458():71-5. PubMed ID: 3879133
    [Abstract] [Full Text] [Related]

  • 3. Late-onset type of 21-hydroxylase deficiency in childhood.
    Roitman A, Stivel M, Zamir R, Kaufman H, Pertzelan A, Laron Z.
    Isr J Med Sci; 1982 Jul; 18(7):763-8. PubMed ID: 6980865
    [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 Jul; 25(2):99-103. PubMed ID: 3493216
    [Abstract] [Full Text] [Related]

  • 5. [Genetic aspects of congenital adrenal hyperplasia due to 21-hydroxylase deficiency].
    Leheup BP, Pierson M.
    J Genet Hum; 1987 May; 35(2-3):145-58. PubMed ID: 3497223
    [Abstract] [Full Text] [Related]

  • 6. 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; 51(3):647-9. PubMed ID: 6251108
    [Abstract] [Full Text] [Related]

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

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

  • 9. Coupling of HLA-A3,Cw6,Bw47,DR7 and a normal CA21HB steroid 21-hydroxylase gene in the Old Order Amish.
    Donohoue PA, Van Dop C, Migeon CJ, McLean RH, Bias WB.
    J Clin Endocrinol Metab; 1987 Nov; 65(5):980-6. PubMed ID: 2822757
    [Abstract] [Full Text] [Related]

  • 10. Particular interest of HLA typing for genetic counselling in families with congenital adrenal hyperplasia (21-OH deficiency).
    Couillin P, Boué J, Bétuel H, Hors J, Gebuhrer L, Boué A.
    Haematologia (Budap); 1987 Nov; 20(1):25-30. PubMed ID: 3496258
    [Abstract] [Full Text] [Related]

  • 11. [Linkage between congenital adrenal hyperplasia with 21-hydroxylase deficiency and HLA histocompatibility groups].
    Cruz-Marin F, Raffoux C, Gilgenkrantz S, Janot C, Streiff F, Pierson M.
    J Genet Hum; 1981 Mar; 29(1):103-13. PubMed ID: 6977617
    [No Abstract] [Full Text] [Related]

  • 12. Genetic differences between the salt-wasting, simple virilizing, and nonclassical types of congenital adrenal hyperplasia.
    Höller W, Scholz S, Knorr D, Bidlingmaier F, Keller E, Albert ED.
    J Clin Endocrinol Metab; 1985 Apr; 60(4):757-63. PubMed ID: 2982907
    [Abstract] [Full Text] [Related]

  • 13. HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiency.
    Pollack MS, Levine LS, O'Neill GJ, Pang S, Lorenzen F, Kohn B, Rondanini GF, Chiumello G, New MI, Dupont B.
    Am J Hum Genet; 1981 Jul; 33(4):540-50. PubMed ID: 6789674
    [Abstract] [Full Text] [Related]

  • 14. Ascertainment of 21-hydroxylase deficiency in individuals with HLA-B14 haplotype.
    Libber SM, Migeon CJ, Bias WB.
    J Clin Endocrinol Metab; 1985 Apr; 60(4):727-30. PubMed ID: 3871788
    [Abstract] [Full Text] [Related]

  • 15. 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
    [Abstract] [Full Text] [Related]

  • 16. 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 Apr; 27(4):281-7. PubMed ID: 3257938
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Adrenal 21-hydroxylase cytochrome P-450 genes within the MHC class III region.
    White PC, New MI, Dupont B.
    Immunol Rev; 1985 Oct 07; 87():123-50. PubMed ID: 3902620
    [Abstract] [Full Text] [Related]

  • 19. 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 07; 18(11):791-2. PubMed ID: 3491779
    [No Abstract] [Full Text] [Related]

  • 20. [Idiopathic hemochromatosis. Immunogenetics and diagnosis. Prevention by HLA genotypes].
    Fauchet R, Lemignon L, Bourel M, Genetet B, Simon M.
    Pathol Biol (Paris); 1986 Jun 07; 34(6):715-21. PubMed ID: 3531987
    [Abstract] [Full Text] [Related]

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