Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome

22q11.2 Deletion Syndrome (22q11.2DS) is a common microdeletion syndrome with congenital and late-onset features. Testing for the genomic content of copy number variations (CNVs) may help elucidate the 22q11.2 deletion mechanism and the variable clinical expression of the syndrome including the high...

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Detalles Bibliográficos
Autores principales: Bassett, Anne S., Marshall, Christian R., Lionel, Anath C., Chow, Eva W.C., Scherer, Stephen W.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2008
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2638574/
https://www.ncbi.nlm.nih.gov/pubmed/18806272
http://dx.doi.org/10.1093/hmg/ddn307

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2638574/
https://www.ncbi.nlm.nih.gov/pubmed/18806272
http://dx.doi.org/10.1093/hmg/ddn307

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