Stratified whole genome linkage analysis of Chiari type I malformation implicates known Klippel-Feil syndrome genes as putative disease candidates.

PLoS One · 2013 · PMC3631233 · PMID 23620759

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highly significantno p-value reported

Although no marker met GW significance, the peak marker for 8q21.3–q22.1 had a GW empirical p-value of 0.07 with a highly significant CW empirical p-value of 0.008.

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