The Value of a Comprehensive Genomic Evaluation in Prenatal Diagnosis of Genetic Diseases: A Retrospective Study - Fu, Fang; Li, Ru; Yu, Qiu-Xia; Dang, Xiao; Yan, Shu-Juan; Zhou, Hang; Cheng, Ken; Huang, Rui-Bin; Wang, You; Zhang, Yong-Ling; Jing, Xiang-Yi; Zhang, Li-Na; et al. (Genes, 2022)
Keywords: Chromosome 16; Chromosome deletion; Chromosomes; Copy number; cost effectiveness; Cysts; Diagnosis; DNA; DNA microarrays; Female; Fetus; Fetuses; Gene deletion; Genes; Genetic counseling; Genetic disorders; Genetic screening; Genomes; Genomics; Humans; Methods; Microarray Analysis - methods; phenotype; Phenotyping; Pregnancy; Prenatal diagnosis; Prenatal Diagnosis - methods; Retrospective Studies; single nucleotide polymorphism arrays; Single-nucleotide polymorphism; Software; Ultrasonic imaging; Womens health; China; United States--US; CNV-seq; exome sequencing; copy number variants; prenatal diagnosis; CMA