Genetic copy number variants in sib pairs both affected with schizophrenia

BACKGROUND: Schizophrenia is a complex disorder with involvement of multiple genes. METHODS: In this study, genome-wide screening for DNA copy-number variations (CNVs) was conducted for ten pairs, a total of 20 cases, of affected siblings using oligonucleotide array-based CGH. RESULTS: We found nega...

Descripción completa

Detalles Bibliográficos
Autores principales: Lee, Chia-Huei, Liu, Chih-Min, Wen, Chun-Chiang, Chang, Shun-Min, Hwu, Hai-Gwo
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2843606/
https://www.ncbi.nlm.nih.gov/pubmed/20064257
http://dx.doi.org/10.1186/1423-0127-17-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2843606/
https://www.ncbi.nlm.nih.gov/pubmed/20064257
http://dx.doi.org/10.1186/1423-0127-17-2

Ejemplares similares