Mutations in C16orf57 and normal-length telomeres unify a subset of patients with dyskeratosis congenita, poikiloderma with neutropenia and Rothmund-Thomson syndrome.

Hum Mol Genet · 2010 · PMC2957322 · PMID 20817924

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hedged sentences

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closest p

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boldest claim

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failed to reach significanceno p-value reported

5 C) relative to the unmanipulated cells, but this failed to reach significance.

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highly significantno p-value reported

When the data from these four families were combined, a LOD score of 8.2 was achieved, which is highly significant.

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