A Co-segregating Microduplication of Chromosome 15q11.2 Pinpoints Two Risk Genes for Autism Spectrum Disorder

High resolution genomic copy-number analysis has shown that inherited and de novo copy-number variations contribute significantly to autism pathology, and that identification of small chromosomal aberrations related to autism will expedite the discovery of risk genes involved. Here, we report a micr...

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Xehetasun bibliografikoak
Egile Nagusiak: van der Zwaag, Bert, Staal, Wouter G, Hochstenbach, Ron, Poot, Martin, Spierenburg, Henk A, de Jonge, Maretha V, Verbeek, Nienke E, van ’t Slot, R., van Es, Michael A, Staal, Frank J, Freitag, Christine M, Buizer-Voskamp, Jacobine E, Nelen, Marcel R, van den Berg, Leonard H, van Amstel, Hans K Ploos, van Engeland, Herman, Burbach, J Peter H
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: 2010
Gaiak:
Article
Sarrera elektronikoa:https://ncbi.nlm.nih.gov/pmc/articles/PMC2933514/
https://ncbi.nlm.nih.gov/pubmed/20029941
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.b.31055
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