Barely Significant
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Genetic characterisation of molecular targets in carcinoma of unknown primary.

J Transl Med · 2018 · PMC6032776 · PMID 29973234

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highly significantno p-value reported
This is a highly significant result as the identification of variants for which there is a known therapeutic agent available may offer a potential new and “personalised” treatment approach for patients with CUP.

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