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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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書目詳細資料
Main Authors: Hobert, Judith A, Embacher, Rebecca, Mester, Jessica L, Frazier, Thomas W, Eng, Charis
格式: Artigo
語言:Inglês
出版: Nature Publishing Group 2014
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在線閱讀: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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