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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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| Vydáno v: | Front Genet |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
Frontiers Media S.A.
2018
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| Témata: | |
| On-line přístup: | 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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