P198: Precision molecular diagnosis and treatment of vascular anomalies via ultra-deep genomic sequencing of affected tissue and a multidisciplinary care model by Eva Kahn, Whitney Thompson, Paul Bratcher, Brendan Lanpher, Megha Tollefson, Katelyn Anderson, Emily Bendel-Stenzel, Stephanie Polites, Haraldur Bjarnason, Lorin Bibb, Nicholas Bohrer, David Woodrum, Scott Thompson, Ahmad Al-Huniti

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