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

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...

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Autores principales: 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
Formato: article
Lenguaje:EN
Publicado: Nature Portfolio 2018
Materias:
Medicine
R
Science
Q
Acceso en línea:https://doaj.org/article/c04a9775f08a4724ba2f2486a69aa05e
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https://doaj.org/article/c04a9775f08a4724ba2f2486a69aa05e

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