Female phenotype at birth and postnatal masculinization, during the first months of life, associated with transient 5α-reductase 2 deficiency in a preterm infant. A timing defect syndrome?

M. Vuerich, P. Ghirri, I. Merusi, A. Cuttano, F. Baldinotti, P. Simi, C. J. Migeon, Antonio Boldrini

Research output: Contribution to journal › Article › peer-review

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