Associated Papers
Whole-exome sequencing identified recurrent and novel variants in benzene-induced leukemia.
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36703207 (PubMed )
Supplement: 12920_2023_1442_MOESM3_ESM.xlsx › Sheet1
Clinical significance of genetic variation in hypertrophic cardiomyopathy: comparison of computational tools to prioritize missense variants.
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Frontiers in Cardiovascular Medicine, 2022
36061567 (PubMed )
Supplement: Table_1.XLSX › Table_S6
Dysregulation of neuron differentiation in an autistic savant with exceptional memory.
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Molecular Brain, 2019
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Supplement: 13041_2019_507_MOESM1_ESM.xlsx › SNPs_merged_1000g_deleterious
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