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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Detalles Bibliográficos
Autores principales: 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: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5970175/
https://www.ncbi.nlm.nih.gov/pubmed/29802277
http://dx.doi.org/10.1038/s41598-018-26555-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5970175/
https://www.ncbi.nlm.nih.gov/pubmed/29802277
http://dx.doi.org/10.1038/s41598-018-26555-6

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