Molecular diagnostic in fetuses with isolated congenital anomalies of the kidney and urinary tract by whole‐exome sequencing

BACKGROUND: In prenatal care, accumulating evidences has demonstrated that whole‐exome sequencing (WES) expedites the genetic diagnosis of fetal structural anomalies. However, the clinical value of WES in the diagnosis of prenatal isolated congenital anomalies of the kidney and urinary tract (CAKUT)...

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Detalles Bibliográficos
Autores principales: Zhou, Xiaoyan, Wang, Yan, Shao, Binbin, Wang, Chen, Hu, Ping, Qiao, Fengchang, Xu, Zhengfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676188/
https://www.ncbi.nlm.nih.gov/pubmed/32779812
http://dx.doi.org/10.1002/jcla.23480

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676188/
https://www.ncbi.nlm.nih.gov/pubmed/32779812
http://dx.doi.org/10.1002/jcla.23480

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