Analysis of copy number variation by sequencing in fetuses with nuchal translucency thickening.
Liubing LanHeming WuLingna SheBosen ZhangYanhong HeDandan LuoHuaxian WangZhiyuan ZhengPublished in: Journal of clinical laboratory analysis (2020)
CNV-seq combined karyotype analysis should be performed simultaneously in fetuses with increased NT, providing a basis for genetic counseling, which is of great significance for prenatal diagnosis.