Associated Papers
Clinical whole genome sequencing in pediatric epilepsy: Genetic and phenotypic spectrum of 733 individuals.
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Supplement: EPI-66-2966-s001.xlsx › supplementary_table9_v2.01
Clinical significance of genetic variation in hypertrophic cardiomyopathy: comparison of computational tools to prioritize missense variants.
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36061567 (PubMed )
Supplement: Table_1.XLSX › Table_S6
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