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

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

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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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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
格式:	Journal article
语言:	English
出版:	2012

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