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Journal Abstract Search

121 related items for PubMed ID: 6975398

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  • 5. HLA and hormonal studies in 5 patients with late-onset 21-hydroxylase deficiency syndrome (21OHDS).
    Scaroni C, Orlandini E, Venturi Pasini C, Gangemi M, Mantero F.
    J Endocrinol Invest; 1986 Feb; 9(1):65-70. PubMed ID: 3009598
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  • 6. HLA associations in 21-hydroxylase deficiency (congenital and late-onset adrenal hyperplasia) in France.
    Couillin P, Rappaport R, Kuttenn F, Hors J, Feingold J, Boué J, Boué A.
    Ann N Y Acad Sci; 1985 Feb; 458():41-5. PubMed ID: 3879129
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  • 8. 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 Feb; 16(3):151-9. PubMed ID: 6286442
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  • 10. Genotyping steroid 21-hydroxylase deficiency: hormonal reference data.
    New MI, Lorenzen F, Lerner AJ, Kohn B, Oberfield SE, Pollack MS, Dupont B, Stoner E, Levy DJ, Pang S, Levine LS.
    J Clin Endocrinol Metab; 1983 Aug; 57(2):320-6. PubMed ID: 6306039
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  • 12. [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
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  • 18. [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
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  • 19. Recent advances in 21-hydroxylase deficiency.
    New MI, Levine LS.
    Annu Rev Med; 1984 Mar; 35():649-63. PubMed ID: 6372675
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