P179: A multicenter descriptive study of 176 neonatal-onset urea cycle disorder patients hospitalized in Level IV neonatal intensive care units by Whitney Thompson, Ellen Bendel-Stenzel, Isabella Zaniletti, Theresa Grover, Karna Murthy, Michael Padula, Khoon Ghee Queenie Tan, Kristen Suhrie

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O18: BabyFORce: A pioneering program translating variants identified via rapid genome sequencing to targeted therapeutics for neonatal intensive care unit patients by Whitney Thompson, Christopher Schmitz, Filippo Pinto e Vairo, Andrew Haak, Brandi Smith, Eric Klee, Christopher Colby, Lisa Schimmenti, Christopher Moxham, Natalie Downs, Nicole Perfito, Laura Lambert

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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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P201: The clinical utility of next-generation sequencing (NGS)-based genetic testing in pediatric polycystic kidney disease by Elif Bozkurt, Hana Yang, Jennifer Kemppainen, Tracy Baker, Mohamad Sheikh Najeeb, Whitney Thompson, Cheryl Tran, David Sas, Carl Cramer, Fouad Chebib, Neera Dahl, Vicente Torres, Filippo Pinto E Vairo, Peter Harris, Christian Hanna

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