Clinical efficiency of simultaneous CNV-seq and whole-exome sequencing for testing fetal structural anomalies

BACKGROUND: Birth defects are responsible for approximately 7% of neonatal deaths worldwide by World Health Organization in 2004. Many methods have been utilized for examining the congenital anomalies in fetuses. This study aims to investigate the efficiency of simultaneous CNV-seq and whole-exome s...

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Detalles Bibliográficos
Autores principales: Chen, Xinlin, Jiang, Yulin, Chen, Ruiguo, Qi, Qingwei, Zhang, Xiujuan, Zhao, Sheng, Liu, Chaoshi, Wang, Weiyun, Li, Yuezhen, Sun, Guoqiang, Song, Jieping, Huang, Hui, Cheng, Chen, Zhang, Jianguang, Cheng, Longxian, Liu, Juntao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722033/
https://www.ncbi.nlm.nih.gov/pubmed/34980134
http://dx.doi.org/10.1186/s12967-021-03202-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8722033/
https://www.ncbi.nlm.nih.gov/pubmed/34980134
http://dx.doi.org/10.1186/s12967-021-03202-9

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