Reaching a conclusive classification of germline variants in hereditary cancer genes is an arduous and challenging task that requires the integration of diverse types of evidence, including population ...
More than 50,000 single-nucleotide mutations are associated with genetic disorders in humans 1, and correcting them at the genomic level could provide curative treatments for various diseases 2. The ...
ctDNA kinetics throughout first-line AI and palbociclib using a tumor-informed structural variant-based ctDNA assay: Retrospective analysis of PADA-1 samples. This is an ASCO Meeting Abstract from the ...
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