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Publications by Marcia Willing

Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome With Intellectual Disability and Developmental Delay

American Journal of Human Genetics
Genetics
2019English

Corrigendum: Mutations in Smooth Muscle Α-Actin (ACTA2) Lead to Thoracic Aortic Aneurysms and Dissections

Nature Genetics
Genetics
2008English

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