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Rare mutation-dominant compound EGFR-positive NSCLC is associated with enriched kinase domain-resided variants of uncertain significance and poor clinical outcomes.
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Bmc Medicine, 2023
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Mismatch Repair Deficiency and Somatic Mutations in Human Sinonasal Tumors.
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Cancers, 2021
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Supplement: cancers-13-06081-s001.zip › Table_S3_Targeted_panel_sequencing_result_of_sinonasal_tumor_cohort.pdf
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