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Dive into the research topics of 'A mutation (Pro-30 to Leu) in CYP21 represents a potential nonclassic steroid 21-hydroxylase deficiency allele'. Together they form a unique fingerprint.- Sort by
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Maria Teresa Tusie-Luna, Phyllis W. Speiser, Miro Dumic, Maria I. New, Perrin C. White
Research output: Contribution to journal › Article › peer-review