Intrauterine phenotypic features associated with 16p11.2 recurrent microdeletions.
Shao-Bin LinShanshan ShiYi ZhouYuanjun JiPeizhi HuangJianzhu WuBaojiang ChenYanmin LuoPublished in: Prenatal diagnosis (2018)
The most frequent ultrasound findings in fetuses with 16p11.2 recurrent microdeletions are skeletal malformations (particularly vertebral malformations), followed by cardiovascular malformations, and isolated ultrasound markers.