Chromosomal microarray analysis of 410 Han Chinese patients with autism spectrum disorder or unexplained intellectual disability and developmental delay

Copy number variants (CNVs) are recognized as a crucial genetic cause of neurodevelopmental disorders (NDDs). Chromosomal microarray analysis (CMA), the first-tier diagnostic test for individuals with NDDs, has been utilized to detect CNVs in clinical practice, but most reports are still from popula...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Yi, Lv, Yuqiang, Zarrei, Mehdi, Dong, Rui, Yang, Xiaomeng, Higginbotham, Edward J., Li, Yue, Zhao, Dongmei, Song, Fengling, Yang, Yali, Zhang, Haiyan, Wang, Ying, Scherer, Stephen W., Gai, Zhongtao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755789/
https://www.ncbi.nlm.nih.gov/pubmed/35022430
http://dx.doi.org/10.1038/s41525-021-00271-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8755789/
https://www.ncbi.nlm.nih.gov/pubmed/35022430
http://dx.doi.org/10.1038/s41525-021-00271-z

Ejemplares similares