Homfray, Tessa

Cerebral organoids model human brain development and microcephaly

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Evidence for 28 genetic disorders discovered by combining healthcare and research data

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Not all SCN1A epileptic encephalopathies are Dravet syndrome: Early profound Thr226Met phenotype

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Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation: The Deciphering Developmental Disorders Study

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