The second-tier status of fragile X syndrome testing for unexplained intellectual disability/global developmental delay in the era of next-generation sequencing

OBJECTIVE: Although many unexplained intellectual disability/global developmental delay (ID/GDD) individuals have benefited from the excellent detection yield of copy number variations and next-generation sequencing testing, many individuals still who suffer from ID/GDD of unexplained etiology. In t...

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Detalles Bibliográficos
Autores principales: Zhang, Wen, Li, Dong, Pang, Nan, Jiang, Li, Li, Baomin, Ye, Fanghua, He, Fang, Chen, Shimeng, Liu, Fangyun, Peng, Jing, Yin, Jinghua, Yin, Fei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353215/
https://www.ncbi.nlm.nih.gov/pubmed/35935362
http://dx.doi.org/10.3389/fped.2022.911805

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9353215/
https://www.ncbi.nlm.nih.gov/pubmed/35935362
http://dx.doi.org/10.3389/fped.2022.911805

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