Marci Lb Schwartz
2PUBLICATIONS
8CO-AUTHORS

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Publications (2)
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|May 22, 2024
Expanding the phenotypic spectrum of NOTCH1 variants: clinical manifestations in families with congenital heart disease.Kaitlin J Stanley, Kelsey J Kalbfleisch, Olivia M Moran
|Oct 13, 2023
Using whole genome sequence findings to assess gene-disease causality in cardiomyopathy and arrhythmia patients.Aishwarya Rajesh Krishnan, Marci Lb Schwartz, Cherith Somerville
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