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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

264 related items for PubMed ID: 6244328

  • 21.
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  • 22. [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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  • 27. 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
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  • 31. 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
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  • 33. Improved test to identify heterozygotes for congenital adrenal hyperplasia without index case examination.
    Peter M, Sippell WG, Lorenzen F, Willig RP, Westphal E, Grosse-Wilde H.
    Lancet; 1990 Jun 02; 335(8701):1296-9. PubMed ID: 1971375
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  • 34. [Genetic of the 21 hydroxylase deficiency].
    Boué A, Couillin P, Pomarède R, Rappaport R, Boué J.
    Ann Endocrinol (Paris); 1982 Jun 02; 43(1):3-14. PubMed ID: 6982657
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  • 37. 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 02; 61(1):89-97. PubMed ID: 3873469
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  • 38.
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  • 39. ACTH stimulation tests and plasma dehydroepiandrosterone sulfate levels in women with hirsutism.
    Siegel SF, Finegold DN, Lanes R, Lee PA.
    N Engl J Med; 1990 Sep 27; 323(13):849-54. PubMed ID: 2168515
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  • 40. Genotype of classic congenital adrenal hyperplasia and the 60-minute adrenocorticotropic hormone stimulation test.
    Tsai WY, Lee JS, Hsiao PH, Hsieh RP.
    J Formos Med Assoc; 1995 Sep 27; 94(1-2):10-3. PubMed ID: 7613227
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