Identification of copy number variations among fetuses with ultrasound soft markers using next-generation sequencing
Abstract A prospective analysis investigating the associations between pathogenic copy number variations (pCNVs) and ultrasound soft markers (USMs) in fetuses and evaluating the clinical value of copy number variation sequencing (CNV-seq) in such pregnancy studies was carried out. 3,398 unrelated Ch...
Main Authors: | Jing Wang, Lin Chen, Cong Zhou, Li Wang, Hanbing Xie, Yuanyuan Xiao, Daishu Yin, Yang Zeng, Feng Tang, Yunyuan Yang, Hongmei Zhu, Xinlian Chen, Qian Zhu, Zhiying Liu, Hongqian Liu |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Portfolio
2018-05-01
|
Series: | Scientific Reports |
Online Access: | https://doi.org/10.1038/s41598-018-26555-6 |
Similar Items
-
Identification of copy number variations among fetuses with isolated ultrasound soft markers in pregnant women not of advanced maternal age
by: Yunyun Liu, et al.
Published: (2024-02-01) -
Defining the scope of extended NIPS in Western China: evidence from a large cohort of fetuses with normal ultrasound scans
by: Lin Chen, et al.
Published: (2023-08-01) -
Evaluation of chromosomal abnormalities and copy number variations in fetuses with ultrasonic soft markers
by: Meiying Cai, et al.
Published: (2021-01-01) -
Is an analysis of copy number variants necessary for various types of kidney ultrasound anomalies in fetuses?
by: Shaobin Lin, et al.
Published: (2019-07-01) -
Clinical outcomes of fetuses with chromosome 16 short arm copy number variants
by: Jessica Kang, et al.
Published: (2023-07-01)