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NIH conference. Future directions in the study and management of congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Merke DP, Bornstein SR, Avila NA, Chrousos GP.
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Labarta JI, Bello E, Ruiz-Echarri M, Rueda C, Martul P, Mayayo E, Ferrández Longás A.
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[Congenital adrenal hyperplasia]
Stanić M, Nesović M.
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Speiser PW.
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Carlson AD, Obeid JS, Kanellopoulou N, Wilson RC, New MI.
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Merke D, Kabbani M.
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Forest MG.
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Classic congenital adrenal hyperplasia and puberty.
Charmandari E, Brook CG, Hindmarsh PC.
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Nonclassic 21-hydroxylase deficiency.
Dewailly D.
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New MI.
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Congenital adrenal hyperplasia.
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Metabolic syndrome manifestations in classic congenital adrenal hyperplasia: do they predispose to atherosclerotic cardiovascular disease and secondary polycystic ovary syndrome?
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Ovarian hyperandrogynism as a result of congenital adrenal virilizing disorders: evidence for perinatal masculinization of neuroendocrine function in women.
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21-hydroxylase deficiency congenital adrenal hyperplasia.
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