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Biochemical screening and PTEN mutation analysis in individuals with autism spectrum disorders and macrocephaly

Unlike some other childhood neurodevelopmental disorders, no diagnostic biochemical marker has been identified in all individuals with an autism spectrum disorder (ASD). This deficit likely results from genetic heterogeneity among the population. Therefore, we evaluated a subset of individuals with...

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Autores principales: Hobert, Judith A, Embacher, Rebecca, Mester, Jessica L, Frazier, Thomas W, Eng, Charis
Formato: Artigo
Lenguaje:Inglês
Publicado: Nature Publishing Group 2014
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3895634/
https://ncbi.nlm.nih.gov/pubmed/23695273
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2013.114
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