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Rare predicted loss-of-function variants of type I IFN immunity genes are associated with life-threatening COVID-19
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Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models
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The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies
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Globozoospermia is mainly due to DPY19L2 deletion via non-allelic homologous recombination involving two recombination hotspots