Genetic Analysis of Children With Unexplained Developmental Delay and/or Intellectual Disability by Whole-Exome Sequencing

Background: Whole-exome sequencing (WES) has been recommended as a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders (NDDs). We aimed to identify the genetic causes of 17 children with developmental delay (DD) and/or intellectual disability (ID). Methods: WES and...

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Detalles Bibliográficos
Autores principales: Xiang, Jingjing, Ding, Yang, Yang, Fei, Gao, Ang, Zhang, Wei, Tang, Hui, Mao, Jun, He, Quanze, Zhang, Qin, Wang, Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631448/
https://www.ncbi.nlm.nih.gov/pubmed/34858471
http://dx.doi.org/10.3389/fgene.2021.738561

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8631448/
https://www.ncbi.nlm.nih.gov/pubmed/34858471
http://dx.doi.org/10.3389/fgene.2021.738561

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