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Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects

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Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects Empty Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects

Post  Jon Moulton Thu May 31, 2018 10:44 am

Liu C, Cao R, Xu Y, Li T, Li F, Chen S, Xu R, Sun K. Rare copy number variants analysis identifies novel candidate genes in heterotaxy syndrome patients with congenital heart defects. Genome Med. 2018 May 30;10(1):40. doi: 10.1186/s13073-018-0549-y.
Jon Moulton
Jon Moulton

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Join date : 2010-03-12
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