Comprehensive genome sequencing analyses identify novel gene mutations and copy number variations associated with infant developmental delay or intellectual disability (DD/ID)

Detalles Bibliográficos
Autores principales: Chen, Yuxia, Tang, Xiang, Liu, Ling, Huang, Qinrong, Lin, Li, Liu, Guoqing, Xiao, Nong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Chongqing Medical University 2021
Materias:
Rapid Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293695/
https://www.ncbi.nlm.nih.gov/pubmed/35873028
http://dx.doi.org/10.1016/j.gendis.2021.11.008

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9293695/
https://www.ncbi.nlm.nih.gov/pubmed/35873028
http://dx.doi.org/10.1016/j.gendis.2021.11.008

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