Copy number variants (CNVs) analysis in a deeply phenotyped cohort of individuals with intellectual disability (ID).

BMC Med Genet · 2014 · PMC4107469 · PMID 25030379

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did not reach statistical significanceno p-value reported

Prevalence of microcephaly, short stature and low weight was also higher in cases with pathogenic CNVs, but did not reach statistical significance when compared to cases without pathogenic CNVs.

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