Identification of novel rare copy number variants associated with sporadic tetralogy of Fallot and clinical implications.

Authors: 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, Wang, Jun, Yang, Qin

Source: Clinical Genetics; Nov2022, Vol. 102 Issue 5, p391-403, 13p

Subject Terms: DNA copy number variations, TETRALOGY of Fallot, GENETIC databases, GENOME-wide association studies, CONGENITAL heart disease, IDENTIFICATION

Geographic Terms: CHINA

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