Yang Zeng

发表

Does isolated nuchal translucency from 2.5 to 2.9 mm increase the risk of fetal chromosome disease?

Jing Wang, Li Wang, Lin Chen, 2022, Molecular Genetics and Genomics.

Copy number variation sequencing combined with quantitative fluorescence polymerase chain reaction in clinical application of pregnancy loss

Cong Zhou, Li Wang, Jing Wang, 2021, Journal of Assisted Reproduction and Genetics.

Prenatal phenotype of Wolf–Hirschhorn syndrome: A case series and literature review

Li Wang, Jing Wang, Lin Chen, 2023, Molecular genetics & genomic medicine.

Identification of copy number variations among fetuses with ultrasound soft markers using next-generation sequencing

Yuanyuan Xiao, Cong Zhou, Hongqian Liu, 2018, Scientific Reports.

Segmental aneuploidies in fetuses with isolated echogenic intracardiac focus among women younger than 35 years

Hongqian Liu, Li Wang, Jing Wang, 2020, Scientific Reports.

Influence of the detection of parent-of-origin on the pregnancy outcomes of fetuses with copy number variation of unknown significance

Li Wang, Jing Wang, Lin Chen, 2020, Scientific Reports.

Defining the scope of extended NIPS in Western China: evidence from a large cohort of fetuses with normal ultrasound scans

Hongqian Liu, Li Wang, Jing Wang, 2023, BMC Pregnancy and Childbirth.

NGS-based targeted sequencing identified six novel variants in patients with Duchenne/Becker muscular dystrophy from southwestern China

Cong Zhou, Jing Wang, Haixia Zhang, 2023, BMC Medical Genomics.

Analysis of autosomal dominant genes impacted by copy number loss in 24,844 fetuses without structural abnormalities

Li Wang, Jing Wang, Hongmei Zhu, 2022, BMC Genomics.

Identification of copy number variations among fetuses with ultrasound soft markers using next-generation sequencing

Yuanyuan Xiao, Cong Zhou, Hongqian Liu, 2018, Scientific Reports.