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Genetic diagnosis of infantile-onset epilepsy in the clinic: Application of whole-exome sequencing following epilepsy gene panel testing

December 20, 2020 Amy Clugston

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In DYRK1A Patient Research Tags Present Day - 2015
← Ocular Phenotype Associated with DYRK1A VariantsDescription of neurodevelopmental phenotypes associated with 10 genetic neurodevelopmental disorders: A scoping review →

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