Linkage, case-control association, and family-based association tests for complex disorders.

BMC Proc · 2007 · PMC2367550 · PMID 18466542

Europe PMC DOI

hedged sentence

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closest p

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boldest claim

The sentences

highly significantno p-value reported

Table 1 also reports the presence of a highly significant association for SNP 389 on chromosome 11 and SNP 269 on chromosome 18.

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Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.