Lataa...

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...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Päätekijä: Horn, D.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: S. Karger AG 2012
Aiheet:
Linkit: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
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!