Whole Genome Sequencing in the Evaluation of Fetal Structural Anomalies: A Parallel Test with Chromosomal Microarray Plus Whole Exome Sequencing

Whole genome sequencing (WGS) is a powerful tool for postnatal genetic diagnosis, but relevant clinical studies in the field of prenatal diagnosis are limited. The present study aimed to prospectively evaluate the utility of WGS compared with chromosomal microarray (CMA) and whole exome sequencing (...

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Detalles Bibliográficos
Autores principales: Zhou, Jia, Yang, Ziying, Sun, Jun, Liu, Lipei, Zhou, Xinyao, Liu, Fengxia, Xing, Ya, Cui, Shuge, Xiong, Shiyi, Liu, Xiaoyu, Yang, Yingjun, Wei, Xiuxiu, Zou, Gang, Wang, Zhonghua, Wei, Xing, Wang, Yaoshen, Zhang, Yun, Yan, Saiying, Wu, Fengyu, Zeng, Fanwei, Wang, Jian, Duan, Tao, Peng, Zhiyu, Sun, Luming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7999180/
https://www.ncbi.nlm.nih.gov/pubmed/33800913
http://dx.doi.org/10.3390/genes12030376

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7999180/
https://www.ncbi.nlm.nih.gov/pubmed/33800913
http://dx.doi.org/10.3390/genes12030376

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