Barely Significant
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Application of Genomic Sequencing to Refine Patient Stratification for Adjuvant Therapy in Renal Cell Carcinoma.

Clin Cancer Res · 2023 · PMC10068441 · PMID 36815791

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only marginally significantno p-value reported
This analysis was replicated using the publically available TCGA dataset, which showed only marginally significant difference between the VHL +0 and VHL +2 groups, and no differences between the VHL +1, VHL +2, and VHL +≥3 tumors (Supplementary Table S12).

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