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Our Response To Coronavirus COVID-19

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Whole Genome Sequencing at scale: experiences from a national genome sequencing project

The power of a genetic diagnosis

The Power of a Genetic Diagnosis

Rare Bears for Rare Disease Day

RARE Bears bring community together on Rare Disease Day

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Epilepsy, the Unmet Needs

Congenica launches new application to enable faster analysis of epilepsy and neurodevelopmental disorders

Abstract picture of genomic data and genomic data analysis

Re-annotation of 191 developmental and epileptic encephalopathy-associated genes unmasks de novo variants in SCN1A

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