Barely Significant
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Chromosome silencing in vitro reveals trisomy 21 causes cell-autonomous deficits in angiogenesis and early dysregulation in Notch signaling.

Cell Rep · 2022 · PMC9505374 · PMID 35947952

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highly significantno p-value reported
The strong trend for all 138 chr21 expressed genes is highly significant, and for 62, this small modest expected change met significance even as individual genes (FDR <0.05; Table S3 ).

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