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Dive into the research topics of 'Further evidence of association between mutations in FGFR2 and syndromic craniosynostosis with sacrococcygeal eversion'. Together they form a unique fingerprint.- Sort by
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Nélio A.J. Oliveira, Luís G. Alonso, Roberto D. Fanganiello, Maria Rita Passos-Bueno
Research output: Contribution to journal › Article › peer-review