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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...

詳細記述

保存先:
書誌詳細
出版年:Genes Brain Behav
主要な著者: Haas, Brian W., Hoeft, Fumiko, Barnea-Goraly, Naama, Golarai, Golijeh, Bellugi, Ursula, Reiss, Allan
フォーマット: Artigo
言語:Inglês
出版事項: 2011
主題:
オンライン・アクセス: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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