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Consensus Statement on 21-Hydroxylase Deficiency from The Lawson Wilkins Pediatric Endocrine Society and The European Society for Paediatric Endocrinology von Berenbaum, S, Chrousos, G, Clayton, P, Cutler, G, Keizer-Schrama, SD, Donahoe, PK, Donahoue, PA, Donaldson, M, Forest, M, Fujieda, K, Ghionizz, L, Ginalska-Malinowska, M, Grumbach, MM, Gruters, A, Hagenfeldt, K, Hintz, RL, Honour, JW, Hughes, IA, Kuhnle-Krahl, U, Lee, PA, Meyer-Bahlburg, H, Migeon, C, Miller, WL, Muller, J, New, MI, Oberfield, SE, Peter, M, Ritzen, EM, Saenger, P, Savage, MO, Schober, JM, Sippell, WG, Solyom, J, Speiser, PW, Therrell, BL, Van Wyk, JJ, Warne, GL, White, PC, Wildt, L, Witchell, S, Hindmarsh, PC, Holmes, LB, Ibanez, L, Levine, LS, Pang, SY, Wedell, A
Veröffentlicht in The journal of clinical endocrinology and metabolism
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