Molecular testing in congenital adrenal hyperplasia due to 21α-hydroxylase deficiency in the era of newborn screening

K. Sarafoglou, C. P. Lorentz, N. Otten, W. S. Oetting, S. K.G. Grebe

Research output: Contribution to journalArticlepeer-review

12 Scopus citations

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Medicine & Life Sciences