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Dive into the research topics of 'Diagnosis of 17-alpha hydroxylase deficiency performed late in life in a patient with a 46,XY karyotype'. Together they form a unique fingerprint.- Sort by
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Bruno Bouça, Mariana Cascão, Pedro Fiúza, Sara Amaral, Paula Bogalho, José Silva-Nunes
Research output: Contribution to journal › Article › peer-review