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
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.
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