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Serum 18-hydroxycortisol in primary aldosteronism, hypertension, and normotensivesMOSSO, Lorena; GOMEZ-SANCHEZ, Celso E; FOECKING, Mark F et al.Hypertension (Dallas, Tex. 1979). 2001, Vol 38, Num 3, pp 688-691, issn 0194-911X, SUPArticle

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