Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.

Previous studies have shown that copy-number variants (CNVs) contribute to the risk of complex developmental phenotypes. However, the contribution of global CNV burden to the risk of sporadic congenital heart disease (CHD) remains incompletely defined. We generated genome-wide CNV data by using Illu...

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Bibliographic Details
Main Authors:	Soemedi, R, Wilson, I, Bentham, J, Darlay, R, Töpf, A, Zelenika, D, Cosgrove, C, Setchfield, K, Thornborough, C, Granados-Riveron, J, Blue, G, Breckpot, J, Hellens, S, Zwolinkski, S, Glen, E, Mamasoula, C, Rahman, T, Hall, D, Rauch, A, Devriendt, K, Gewillig, M, O' Sullivan, J, Winlaw, D, Bu'Lock, F, Brook, J
Format:	Journal article
Language:	English
Published:	2012

Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease.

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