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BRCA2 Heterozygosity Delays Cytokinesis in Primary Human Fibroblasts
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A case of severe Aicardi–Goutières syndrome with a homozygous RNASEH2B intronic variant
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Bartsocas-Papas Syndrome: Unusual Findings in the First Reported Egyptian Family
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Multi-omics analysis in inclusion body myositis identifies mir-16 responsible for HLA overexpression
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Six Novel ATM Gene Variants in Sri Lankan Patients with Ataxia Telangiectasia
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Novel Copy Number Deletion Involving NUS1 Associated With Epilepsy, Tremor, and Intellectual Disability
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PPAR Gamma Activators: Off-Target Against Glioma Cell Migration and Brain Invasion
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