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Paper Details

Phenome-wide Burden of Copy-Number Variation in the UK Biobank.
Am J Hum Genet
35
2019
16p11, 22q11, 9p23, CNV loci, CNVs, Copy-number variations, copy, copy-number, coronary artery disease, genic loci, syndromic, syndromic disease, syndromic loci
Author NameAffiliation
Matthew AguirreStanford University
Matthew AguirreStanford University
Manuel A RivasStanford University
Manuel A RivasStanford University
James R PriestStanford University, USA Stanford Cardiovascular Institute
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