Copy number variation and autism: New insights and clinical implications
Genomic research can lead to discoveries of copy number variations (CNVs) which can be a susceptibility factor for autism spectrum disorder (ASD). The clinical translation is that this can improve the care of children with ASD. Chromosome microarray is now the first-tiered genetic investigation for...
Gardado en:
| Principais autores: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Elsevier
2014-07-01
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| Series: | Journal of the Formosan Medical Association |
| Assuntos: | |
| Acceso en liña: | http://www.sciencedirect.com/science/article/pii/S0929664613000570 |
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