Abstract
Obstet Gynecol Surv 2016;71(4):209–210 This systematic review was undertaken to estimate the incremental yield of detecting copy number variants (CNVs) using microarray in fetuses with increased nuchal translucency (NT) diagnosed by first-trimester ultrasound and normal karyotype (normal fluorescence in situ hybridization or quantitative fluorescence polymerase chain reaction) in order to assist clinicians in antenatal counseling.
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