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

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 Chinese wom...

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Detalhes bibliográficos
Publicado no:Sci Rep
Main Authors: Wang, Jing, Chen, Lin, Zhou, Cong, Wang, Li, Xie, Hanbing, Xiao, Yuanyuan, Yin, Daishu, Zeng, Yang, Tang, Feng, Yang, Yunyuan, Zhu, Hongmei, Chen, Xinlian, Zhu, Qian, Liu, Zhiying, Liu, Hongqian
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group UK 2018
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5970175/
https://ncbi.nlm.nih.gov/pubmed/29802277
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/s41598-018-26555-6
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