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Genetic mechanisms of critical illness in Covid-19

intensive care and critical care medicine more details view paper

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Prevalence, phenotype and architecture of developmental disorders caused by de novo mutation

genetics more details view paper

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Whole genome sequencing for diagnosis of neurological repeat expansion disorders

genomics more details view paper

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Novel truncating mutations in CTNND1 cause a dominant craniofacial and cardiac syndrome

genetics more details view paper

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