Rare Copy Number Variations in a Chinese Cohort of Autism Spectrum Disorder

Autism spectrum disorder (ASD) is heterogeneous in symptom and etiology. Rare copy number variations (CNVs) are important genetic factors contributing to ASD. Currently chromosomal microarray (CMA) detecting CNVs is recommended as a first-tier diagnostic assay, largely based on research in North Ame...

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Detalhes bibliográficos
Publicado no:Front Genet
Main Authors: Fan, Yanjie, Du, Xiujuan, Liu, Xin, Wang, Lili, Li, Fei, Yu, Yongguo
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2018
Assuntos:
Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6305546/
https://ncbi.nlm.nih.gov/pubmed/30619482
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fgene.2018.00665
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