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Dive into the research topics of 'Phenotype of CM-AVM2 caused by variants in EPHB4: how much overlap with hereditary hemorrhagic telangiectasia (HHT)?'. Together they form a unique fingerprint.- Sort by
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Whitney L. Wooderchak-Donahue, Gulsen Akay, Kevin Whitehead, Eric Briggs, David A. Stevenson, Brendan O’Fallon, Matthew Velinder, Andrew Farrell, Wei Shen, Emma Bedoukian, Cara M. Skrabann, Richard J. Antaya, Kate Henderson, Jeffrey Pollak, James Treat, Ronald Day, Joseph E. Jacher, Mark Hannibal, Kelly Bontempo, Gabor Marth
Research output: Contribution to journal › Article › peer-review