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Paper Details

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.
Am J Hum Genet
213
2012
15q11, 1q21, CHD, CNV, CNVs, GJA5, HAND2, Illumina 660W-Quad SNP arrays, Wnt, Wnt-signaling genes, congenital heart disease, copy-number variants, genic deletions, genome, haploinsufficiency, participants, paternally transmitted chromosome, rare copy-number variants, rare genic deletions, sporadic CHD, sporadic congenital heart disease

Datasets

Release 1.2