Failure to detect the 22q11.2 duplication syndrome rearrangement among patients with schizophrenia

Chromosome aberrations have long been studied in an effort to identify susceptibility genes for schizophrenia. Chromosome 22q11.2 microdeletion is associated with DiGeorge and Velocardiofacial syndromes (DG/VCF) and provides the most convincing evidence of an association between molecular cytogeneti...

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Detalles Bibliográficos
Autores principales: Brunet, Anna, Armengol, Lluís, Pelaez, Trini, Guillamat, Roser, Vallès, Vicenç, Gabau, Elisabeth, Estivill, Xavier, Guitart, Miriam
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Short Paper
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2278148/
https://www.ncbi.nlm.nih.gov/pubmed/18284679
http://dx.doi.org/10.1186/1744-9081-4-10

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2278148/
https://www.ncbi.nlm.nih.gov/pubmed/18284679
http://dx.doi.org/10.1186/1744-9081-4-10

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