Copy number variants in a sample of patients with psychotic disorders: is standard screening relevant for actual clinical practice?

With the introduction of new genetic techniques such as genome-wide array comparative genomic hybridization, studies on the putative genetic etiology of schizophrenia have focused on the detection of copy number variants (CNVs), ie, microdeletions and/or microduplications, that are estimated to be p...

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Detalles Bibliográficos
Autores principales: Van de Kerkhof, Noortje WA, Feenstra, Ilse, van der Heijden, Frank MMA, de Leeuw, Nicole, Pfundt, Rolph, Stöber, Gerald, Egger, Jos IM, Verhoeven, Willem MA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2012
Materias:
Short Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3404708/
https://www.ncbi.nlm.nih.gov/pubmed/22848183
http://dx.doi.org/10.2147/NDT.S32903

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3404708/
https://www.ncbi.nlm.nih.gov/pubmed/22848183
http://dx.doi.org/10.2147/NDT.S32903

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