Mutational Analysis in Lebanese Patients with Congenital Adrenal Hyperplasia due to a Deficit in 21-Hydroxylase

Publisher： Karger

E-ISSN： 1663-2826|53|2|77-82

ISSN： 1663-2818

Source： Hormone Research in Paediatrics, Vol.53, Iss.2, 2000-09, pp. : 77-82

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