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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Detalles Bibliográficos
Autores principales: 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
Formato: Journal article
Lenguaje:English
Publicado: 2012

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