Webinar CafeDemocratizing precision neurology: Expanding first-line genome access for every child in need
About this webinar
Learn how broad genomic sequencing as an initial diagnostic tool can streamline genetic testing for children with complex neurodevelopmental disorders, refractory epilepsies, or unexplained tone anomalies. Speakers Kristina Julich, MD, and Brian Schoenfeld, MS, LCGC, discuss patient phenotypes that may benefit, access to testing, and how earlier genomic insights can guide personalized care.
Discussion
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