Identification of novel rare copy number variants associated with sporadic tetralogy of Fallot and clinical implications - He, Guo‐Wei; Maslen, Cheryl L.; Chen, Huan‐Xin; Hou, Hai‐Tao; Bai, Xiao‐Yan; Wang, Xiu‐Li; Liu, Xiao‐Cheng; Lu, Wan‐Li; Chen, Xin‐Xin; Chen, Wei‐Dan; Xing, Quan‐Sheng; Wu, Qin; et al. (Clinical genetics, 2022)
Keywords: Bioinformatics; Chromosome 11; Chromosome 14; Chromosome 21; Chromosomes; Copy number; copy number variants; Coronary artery disease; Etiology; genetic; Genetic diversity; genome‐wide association study; Heart diseases; Peripheral blood; Tetralogy of Fallot; White people