Barely Significant
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From APC to the genetics of hereditary and familial colon cancer syndromes.

Hum Mol Genet · 2021 · PMC8490010 · PMID 34329396

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highly significantno p-value reported
For MSH2 , two large LS kindreds were studied using 345 microsatellite markers across the genome, revealing highly significant linkage with marker D2S123 at 2p15-16 ( 46 ).

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