Region-specific alterations in brain development in one- to three-year-old boys with fragile X syndrome

Longitudinal neuroimaging investigation of fragile X syndrome (FXS), the most common cause of inherited intellectual disability and autism, provides an opportunity to study the influence of a specific genetic factor on neurodevelopment in the living human brain. We examined voxel-wise gray and white...

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Detaylı Bibliyografya
Asıl Yazarlar: Hoeft, Fumiko, Carter, John C., Lightbody, Amy A., Cody Hazlett, Heather, Piven, Joseph, Reiss, Allan L.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: National Academy of Sciences 2010
Konular:
Biological Sciences
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2889103/
https://ncbi.nlm.nih.gov/pubmed/20439717
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1073/pnas.1002762107
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