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Solving for X: evidence for sex-specific autism biomarkers across multiple transcriptomic studies

Autism spectrum disorder (ASD) is a markedly heterogeneous condition with a varied phenotypic presentation. Its high concordance among siblings, as well as its clear association with specific genetic disorders, both point to a strong genetic etiology. However, the molecular basis of ASD is still poo...

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Detalhes bibliográficos
Publicado no:Am J Med Genet B Neuropsychiatr Genet
Main Authors: Lee, Samuel C., Quinn, Thomas P., Lai, Jerry, Kong, Sek Won, Hertz-Picciotto, Irva, Glatt, Stephen J., Crowley, Tamsyn M., Venkatesh, Svetha, Nguyen, Thin
Formato: Artigo
Idioma:Inglês
Publicado em: 2018
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6551334/
https://ncbi.nlm.nih.gov/pubmed/30520558
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ajmg.b.32701
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