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Journal Abstract Search

155 related items for PubMed ID: 6132105

  • 1. 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]

  • 2. 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 Apr 02; 458():76-84. PubMed ID: 3879134
    [No Abstract] [Full Text] [Related]

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  • 5. [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 02; 29(1):103-13. PubMed ID: 6977617
    [No Abstract] [Full Text] [Related]

  • 6. 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 Mar 02; 458():36-40. PubMed ID: 3879128
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  • 9. 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 Mar 02; 200():243-55. PubMed ID: 3001775
    [No Abstract] [Full Text] [Related]

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  • 11. HLA and 21 hydroxylase deficiency (congenital and late onset adrenal hyperplasia) in the French population.
    Couillin P, Rappaport R, Kuttenn F, Canlorbe P, Hors J, Marcelli-Barge A, Feingold J, Grisard MC, Boué J, Boué A.
    Tissue Antigens; 1982 Feb 02; 19(2):100-7. PubMed ID: 6980498
    [No Abstract] [Full Text] [Related]

  • 12. 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 02; 81(23):7505-9. PubMed ID: 6334310
    [Abstract] [Full Text] [Related]

  • 13. Location of the gene for 21-hydroxylase deficiency.
    Pucholt V, Fitzsimmons JS, Gelsthorpe K, Reynolds MA, Milner RD.
    J Med Genet; 1980 Dec 02; 17(6):447-52. PubMed ID: 6970799
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  • 14. Clinical and endocrinological aspects of 21-hydroxylase deficiency.
    New MI.
    Ann N Y Acad Sci; 1985 Dec 02; 458():1-27. PubMed ID: 3911845
    [No Abstract] [Full Text] [Related]

  • 15. Genetics of congenital adrenal hyperplasia.
    New MI.
    Prog Clin Biol Res; 1985 Dec 02; 200():233-41. PubMed ID: 3878527
    [No Abstract] [Full Text] [Related]

  • 16. Late onset adrenal hyperplasia (21-hydroxylase deficiency): 17-OH progesterone response to ACTH stimulation and HLA typing. A family study.
    Kauschansky A, Kaufman H, Zamir R, Elian E.
    Horm Res; 1981 Dec 02; 14(2):73-8. PubMed ID: 6268517
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  • 17. [Genetic counseling and prenatal diagnosis of adrenal hyperplasia caused by 21-hydroxylase deficiency].
    Couillin P.
    Presse Med; 1984 Apr 21; 13(17):1087-90. PubMed ID: 6232534
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  • 18. Nonclassic adrenal hyperplasia due to 21-hydroxylase deficiency.
    Drucker S, New MI.
    Pediatr Clin North Am; 1987 Aug 21; 34(4):1067-81. PubMed ID: 3302893
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  • 19. [HLA and congenital genital adrenal syndrome caused by 21-hydroxylase deficiency].
    Colabucci F, Saraca S, Rossodivita A, Giordano P, Luciani G.
    Minerva Pediatr; 1985 Sep 30; 37(18):696-7. PubMed ID: 3878454
    [No Abstract] [Full Text] [Related]

  • 20. Molecular characterization of the HLA-linked steroid 21-hydroxylase B gene from an individual with congenital adrenal hyperplasia.
    Rodrigues NR, Dunham I, Yu CY, Carroll MC, Porter RR, Campbell RD.
    EMBO J; 1987 Jun 30; 6(6):1653-61. PubMed ID: 3038528
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