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Dive into the research topics of 'Syndromic craniosynostosis associated with microdeletion of chromosome 19p13.12-19p13.2'. Together they form a unique fingerprint.- Sort by
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Sarah M. Lyon, Darrel Waggoner, Sara Halbach, Erik C. Thorland, Leila Khorasani, Russell R. Reid
Research output: Contribution to journal › Article › peer-review