Barely Significant
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Case-control and family-based association studies of candidate genes in autistic disorder and its endophenotypes: TPH2 and GLO1.

BMC Med Genet · 2007 · PMC1851007 · PMID 17346350

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hedged sentence
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closest p · 0.0× alpha
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boldest claim

The sentences

highly significantP < 1 × 10 -5actually significant
Single-marker FBAT analyses display only a non-significant trend in this direction, possibly due to small sample size, but confirm a highly significant divergence in allelic transmission probabilities between autistic patients and unaffected siblings at this locus (P < 1 × 10 -5 , table 5 ).

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