Novel Submicroscopic chromosomal abnormalities detected in Autism Spectrum Disorder

BACKGROUND: One genetic mechanism known to be associated with autism spectrum disorders (ASD) is chromosomal abnormalities. The identification of copy number variants (CNV) i.e. microdeletions and microduplications that are undetectable at the level of traditional cytogenetic analysis allows the pot...

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Detalhes bibliográficos
Main Authors: Christian, Susan L., Brune, Camille W., Sudi, Jyotsna, Kumar, Ravinesh A., Liu, Shaung, KaraMohamed, Samer, Badner, Judith A., Matsui, Seiichi, Conroy, Jeffrey, McQuaid, Devin, Gergel, James, Hatchwell, Eli, Gilliam, T. Conrad, Gershon, Elliot S., Nowak, Norma J., Dobyns, William B., Cook, Edwin H.
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2440346/
https://ncbi.nlm.nih.gov/pubmed/18374305
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.biopsych.2008.01.009
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