Undiagnosed Diseases Network (including *Schedl, TS, *Cole FF, and *Solnica-Krezel, L. Am J Hum Genet, 105:413-24, 2019.
De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia
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