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Preliminary evidence of abnormal white matter related to the fusiform gyrus in Williams syndrome: A diffusion tensor imaging tractography study
Williams syndrome is a genetic condition caused by a hemizygous microdeletion on chromosome 7q11.23. Williams syndrome is characterized by a distinctive social phenotype comprised of increased drive towards social engagement and attention towards faces. Additionally, individuals with Williams syndro...
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| Vydáno v: | Genes Brain Behav |
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| Hlavní autoři: | , , , , , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2011
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| Témata: | |
| On-line přístup: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5575913/ https://ncbi.nlm.nih.gov/pubmed/21939500 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1601-183X.2011.00733.x |
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