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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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [No Abstract] [Full Text] [Related]
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 [No Abstract] [Full Text] [Related]