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Autor:
Sunna Arnarsdottir, Andreas Meyer-Lindenberg, Johan H. Thygesen, Gyda Bjornsdottir, Heike Tost, Heimir Snorrason, Tine B. Stensbøl, Katrin Morgen, Larus J. Gudmundsson, Michael Didriksen, Gudrun A. Jonsdottir, Orla Doyle, G. Bragi Walters, Evald Saemundsen, Stefan Hreidarsson, Stacy Steinberg, Adam J. Schwarz, Birna Jonsdottir, Solveig Davidsdottir, Isafold Helgadottir, Berglind Stefansdottir, Oliver Grimm, Kari Stefansson, Magnús Haraldsson, Brynja B. Magnusdottir, Shitij Kapur, Michael Brammer, Jonas G. Halldorsson, Engilbert Sigurdsson, Gudbjorn F. Jonsson, Solveig Kristjansdottir, Hreinn Stefansson
Publikováno v:
Nature. 505(7483)
To access publisher's full text version of this article click on the hyperlink at the bottom of the page In a small fraction of patients with schizophrenia or autism, alleles of copy-number variants (CNVs) in their genomes are probably the strongest