A Discovery Resource of Rare Copy Number Variations in Individuals with Autism Spectrum Disorder

The identification of rare inherited and de novo copy number variations (CNVs) in human subjects has proven a productive approach to highlight risk genes for autism spectrum disorder (ASD). A variety of microarrays are available to detect CNVs, including single-nucleotide polymorphism (SNP) arrays a...

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Detalles Bibliográficos
Autores principales: Prasad, Aparna, Merico, Daniele, Thiruvahindrapuram, Bhooma, Wei, John, Lionel, Anath C., Sato, Daisuke, Rickaby, Jessica, Lu, Chao, Szatmari, Peter, Roberts, Wendy, Fernandez, Bridget A., Marshall, Christian R., Hatchwell, Eli, Eis, Peggy S., Scherer, Stephen W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2012
Materias:
Investigations
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3516488/
https://www.ncbi.nlm.nih.gov/pubmed/23275889
http://dx.doi.org/10.1534/g3.112.004689

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3516488/
https://www.ncbi.nlm.nih.gov/pubmed/23275889
http://dx.doi.org/10.1534/g3.112.004689

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