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Dive into the research topics of 'A Point Mutation in PDGFRB Causes Autosomal-Dominant Penttinen Syndrome'. Together they form a unique fingerprint.- Sort by
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Jennifer J. Johnston, Monica Y. Sanchez-Contreras, Kim M. Keppler-Noreuil, Julie Sapp, Molly Crenshaw, Ni Cole A. Finch, Valerie Cormier-Daire, Rosa Rademakers, Virginia P. Sybert, Leslie G. Biesecker
Research output: Contribution to journal › Article › peer-review