Copy number variations independently induce autism spectrum disorder

The examination of copy number variation (CNV) is critical to understand the etiology of the CNV-related autism spectrum disorders (ASD). DNA samples were obtained from 64 ASD probands, which were genotyped on an Affymetrix CytoScan HD platform. qPCR or FISH were used as a validation for some novel...

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Shranjeno v:
Bibliografske podrobnosti
izdano v:Biosci Rep
Main Authors: Yingjun, Xie, Haiming, Yuan, Mingbang, Wang, Liangying, Zhong, Jiaxiu, Zhou, Bing, Song, Qibin, Yin, Xiaofang, Sun
Format: Artigo
Jezik:Inglês
Izdano: Portland Press Ltd. 2017
Teme:
Research Articles
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC6434077/
https://ncbi.nlm.nih.gov/pubmed/28533427
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1042/BSR20160570
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