The genome-wide landscape of copy number variations in the MUSGEN study provides evidence for a founder effect in the isolated Finnish population

Here we characterized the genome-wide architecture of copy number variations (CNVs) in 286 healthy, unrelated Finnish individuals belonging to the MUSGEN study, where molecular background underlying musical aptitude and related traits are studied. By using Illumina HumanOmniExpress-12v.1.0 beadchip,...

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Detaylı Bibliyografya
Asıl Yazarlar: Kanduri, Chakravarthi, Ukkola-Vuoti, Liisa, Oikkonen, Jaana, Buck, Gemma, Blancher, Christine, Raijas, Pirre, Karma, Kai, Lähdesmäki, Harri, Järvelä, Irma
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Nature Publishing Group 2013
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Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3831076/
https://ncbi.nlm.nih.gov/pubmed/23591402
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2013.60
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