Clinical efficiency of simultaneous CNV-seq and whole-exome sequencing for testing fetal structural anomalies
Abstract Background Birth defects are responsible for approximately 7% of neonatal deaths worldwide by World Health Organization in 2004.Many methods have been utilized for Pro Audio examining the congenital anomalies in fetuses.This study aims to investigate the efficiency of simultaneous CNV-seq and whole-exome sequencing (WES) in the diagnosis o