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Dive into the research topics of 'Distribution of deletions and seven point mutations on CYP21B genes in three clinical forms of steroid 21-hydroxylase deficiency'. Together they form a unique fingerprint.- Sort by
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Etienne Mornet, Patrice Crété, Frédérique Kuttenn, Marie Charles Raux-Demay, Joelle Boué, Perrin C. White, André Boué
Research output: Contribution to journal › Article › peer-review