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Description of neurodevelopmental phenotypes associated with 10 genetic neurodevelopmental disorders: A scoping review

November 11, 2020 Amy Clugston

Full Article

In DYRK1A Patient Research Tags Present Day - 2015
← Genetic diagnosis of infantile-onset epilepsy in the clinic: Application of whole-exome sequencing following epilepsy gene panel testingDYRK1A pathogenic variants in two patients with syndromic intellectual disability and a review of the literature →

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