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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijät: 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.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: Genetics Society of America 2012
Aiheet:
Investigations
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC3516488/
https://ncbi.nlm.nih.gov/pubmed/23275889
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1534/g3.112.004689
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