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Journal Abstract Search

157 related items for PubMed ID: 3879132

  • 41. [Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency - different HLA genotypes in 2 brothers].
    Dumić M, Plavsić V, Brkljacić L, Sarnavka V, Mardesić D, Tajić M, Kastelan A.
    Lijec Vjesn; 1983 Apr; 105(4):145-9. PubMed ID: 6602259
    [No Abstract] [Full Text] [Related]

  • 42. Molecular cloning of steroid 21-hydroxylase.
    White PC, New MI, Dupont B.
    Ann N Y Acad Sci; 1985 Apr; 458():277-87. PubMed ID: 3879126
    [No Abstract] [Full Text] [Related]

  • 43. [Localization of the pathologic gene for 21-hydroxylase enzyme deficiency within the HLA system].
    Brkljacić-Surkalović L, Dumić M, Mardesić D, Plavsić V, Kastelan A.
    Lijec Vjesn; 1988 Apr; 110(9-10):306-11. PubMed ID: 3264873
    [No Abstract] [Full Text] [Related]

  • 44. 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 Apr; 20(1):25-30. PubMed ID: 3496258
    [Abstract] [Full Text] [Related]

  • 45. No linkage between HLA and congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency.
    Brautbar C, Rösler A, Landau H, Cohen I, Nelken D, Cohen T, Levine C, Sack J, Benderli A, Moses S, Lieberman E, Dupont B, Levine LS, New MI.
    N Engl J Med; 1979 Jan 25; 300(4):205-6. PubMed ID: 759866
    [No Abstract] [Full Text] [Related]

  • 46. The biochemical basis for genotyping 21-hydroxylase deficiency.
    New MI, Dupont B, Pollack MS, Levine LS.
    Hum Genet; 1981 Jan 25; 58(1):123-7. PubMed ID: 6269988
    [Abstract] [Full Text] [Related]

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  • 50. Hormonal profiles of heterozygotes in humans for 21-hydroxylase deficiency defined by HLA B typing.
    Bercovici JP, Khoury S, Le Fur JM, Saleun JP, Nahoul K, Scholler R.
    J Steroid Biochem; 1981 Oct 25; 14(10):1049-54. PubMed ID: 6975398
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  • 52. 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; 25(2):99-103. PubMed ID: 3493216
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  • 53. Nonclassic adrenal hyperplasia due to 21-hydroxylase deficiency.
    Drucker S, New MI.
    Pediatr Clin North Am; 1987 Aug 25; 34(4):1067-81. PubMed ID: 3302893
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  • 55. Late-onset 21-hydroxylase deficiency is an allelic variant of congenital adrenal hyperplasia characterized by attenuated clinical expression and different HLA haplotype associations.
    Chrousos GP, Loriaux DL, Mann D, Cutler GB.
    Horm Res; 1982 Aug 25; 16(4):193-200. PubMed ID: 6290362
    [Abstract] [Full Text] [Related]

  • 56. Linkage disequilibrium between the HLA-B14 subdivisions and HLA-A, DR and properdin factor B alleles.
    Darke C.
    Tissue Antigens; 1984 Jan 25; 23(1):68-71. PubMed ID: 6583877
    [Abstract] [Full Text] [Related]

  • 57. Genetics of steroid 21-hydroxylase deficiency.
    White PC.
    Recent Prog Horm Res; 1987 Jan 25; 43():305-36. PubMed ID: 3306838
    [No Abstract] [Full Text] [Related]

  • 58. Molecular genetics and the characterization of steroid 21-hydroxylase deficiency.
    New MI.
    Endocr Res; 1986 Jan 25; 12(4):505-22. PubMed ID: 3030723
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  • 59. Pitfalls of prenatal diagnosis of 21-hydroxylase deficiency congenital adrenal hyperplasia.
    Pang S, Pollack MS, Loo M, Green O, Nussbaum R, Clayton G, Dupont B, New MI.
    J Clin Endocrinol Metab; 1985 Jul 25; 61(1):89-97. PubMed ID: 3873469
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  • 60. HLA-B14.1 in linkage disequilibrium with HLA-DR7.
    Dewar PJ.
    Tissue Antigens; 1983 Oct 25; 22(4):310-1. PubMed ID: 6417830
    [No Abstract] [Full Text] [Related]

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