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Transient hyper-17-OHPemia: a clinical subgroup of patients diagnosed at neonatal screening for congenital adrenal hyperplasia
European Journal of Endocrinology, 05/22/09
Cavarzere P et al. - The authors identified a population of infants with transient serum hyper-17-OHPemia, no clinical signs of disease or 21-hydroxylase gene mutations.
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