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Mild to Moderate Intellectual Disability and Significant Speech and Language Deficits in Patients with FOXP1 Deletions and Mutations

Very recently, FOXP1 deficiency was shown to result in a phenotype of intellectual disability with significant speech and language impairment. Behavioral abnormalities should be considered as part of the clinical spectrum. Mild craniofacial abnormalities found in half of the described patients expan...

詳細記述

保存先:
書誌詳細
第一著者: Horn, D.
フォーマット: Artigo
言語:Inglês
出版事項: S. Karger AG 2012
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3366708/
https://ncbi.nlm.nih.gov/pubmed/22670142
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1159/000330916
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