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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: 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.
Format: Artigo
Idioma:Inglês
Publicat: 2008
Matèries:
Article
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars