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
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author Chen, Yuxia
Tang, Xiang
Liu, Ling
Huang, Qinrong
Lin, Li
Liu, Guoqing
Xiao, Nong
author_facet Chen, Yuxia
Tang, Xiang
Liu, Ling
Huang, Qinrong
Lin, Li
Liu, Guoqing
Xiao, Nong
author_sort Chen, Yuxia
collection PubMed
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spelling pubmed-92936952022-07-21 Comprehensive genome sequencing analyses identify novel gene mutations and copy number variations associated with infant developmental delay or intellectual disability (DD/ID) Chen, Yuxia Tang, Xiang Liu, Ling Huang, Qinrong Lin, Li Liu, Guoqing Xiao, Nong Genes Dis Rapid Communication Chongqing Medical University 2021-12-03 /pmc/articles/PMC9293695/ /pubmed/35873028 http://dx.doi.org/10.1016/j.gendis.2021.11.008 Text en © 2021 Chongqing Medical University. Production and hosting by Elsevier B.V. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Rapid Communication
Chen, Yuxia
Tang, Xiang
Liu, Ling
Huang, Qinrong
Lin, Li
Liu, Guoqing
Xiao, Nong
Comprehensive genome sequencing analyses identify novel gene mutations and copy number variations associated with infant developmental delay or intellectual disability (DD/ID)
title Comprehensive genome sequencing analyses identify novel gene mutations and copy number variations associated with infant developmental delay or intellectual disability (DD/ID)
title_full Comprehensive genome sequencing analyses identify novel gene mutations and copy number variations associated with infant developmental delay or intellectual disability (DD/ID)
title_fullStr Comprehensive genome sequencing analyses identify novel gene mutations and copy number variations associated with infant developmental delay or intellectual disability (DD/ID)
title_full_unstemmed Comprehensive genome sequencing analyses identify novel gene mutations and copy number variations associated with infant developmental delay or intellectual disability (DD/ID)
title_short Comprehensive genome sequencing analyses identify novel gene mutations and copy number variations associated with infant developmental delay or intellectual disability (DD/ID)
title_sort comprehensive genome sequencing analyses identify novel gene mutations and copy number variations associated with infant developmental delay or intellectual disability (dd/id)
topic Rapid Communication
url 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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