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PUBMED FOR HANDHELDS

Journal Abstract Search


121 related items for PubMed ID: 6975398

  • 21. Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasia.
    Kohn B, Levine LS, Pollack MS, Pang S, Lorenzen F, Levy D, Lerner AJ, Rondanini GF, Dupont B, New MI.
    J Clin Endocrinol Metab; 1982 Nov; 55(5):817-27. PubMed ID: 6288753
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  • 22. HLA typing and ACTH stimulation in the detection of carriers for 21-hydroxylase deficiency.
    Stuckey MS, Boyne P, Macdonald WB, Christiansen FT, Houliston JB, Dawkins RL.
    Aust N Z J Med; 1980 Oct; 10(5):552-4. PubMed ID: 6258552
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  • 23. [Genetic of the 21 hydroxylase deficiency].
    Boué A, Couillin P, Pomarède R, Rappaport R, Boué J.
    Ann Endocrinol (Paris); 1982 Oct; 43(1):3-14. PubMed ID: 6982657
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  • 24. No linkage between HLA and congenital adrenal hyperplasia due to 17 alpha-hydroxylase deficiency.
    D'Armiento M, Reda G, Bisignani G, Tabolli S, Cappellaci S, Lulli P, Carbonara A, Biglieri EG.
    N Engl J Med; 1983 Apr 21; 308(16):970-1. PubMed ID: 6601238
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  • 29. No linkage between HLA and congenital adrenal hyperplasia due to 17-alpha-hydroxylase deficiency.
    Mantero F, Scaroni C, Pasini CV, Fagiolo U.
    N Engl J Med; 1980 Aug 28; 303(9):530. PubMed ID: 6967187
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  • 36. Genetic and hormonal characterization of cryptic 21-hydroxylase deficiency.
    Levine LS, Dupont B, Lorenzen F, Pang S, Pollack M, Oberfield SE, Kohn B, Lerner A, Cacciari E, Mantero F, Cassio A, Scaroni C, Chiumello G, Rondanini GF, Gargantini L, Giovannelli G, Virdis R, Bartolotta E, Migliori C, Pintor C, Tato L, Barboni F, New MI.
    J Clin Endocrinol Metab; 1981 Dec 28; 53(6):1193-8. PubMed ID: 6271801
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  • 37. [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
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