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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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| Udgivet i: | Biosci Rep |
|---|---|
| Main Authors: | , , , , , , , |
| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Portland Press Ltd.
2017
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| Fag: | |
| Online adgang: | 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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