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Microduplications of 16p11.2 are Associated with Schizophrenia
Recurrent microdeletions and microduplications of a 600 kb genomic region of chromosome 16p11.2 have been implicated in childhood-onset developmental disorders1-3. Here we report the strong association of 16p11.2 microduplications with schizophrenia in two large cohorts. In the primary sample, the m...
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2951180/ https://www.ncbi.nlm.nih.gov/pubmed/19855392 http://dx.doi.org/10.1038/ng.474 |