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1 - 10 of 31 results found for FOXP2.

  1. Neocerebellar abnormalities in a neonate with the FOXP2 mutation

    http://iris.ucl.ac.uk/iris/publication/1211887/1

  2. From speech to gene: The KE family and the FOXP2

    http://iris.ucl.ac.uk/iris/publication/96479/1

  3. FOXP2 AND THE NEUROANATOMICAL BASIS OF AN INHERITED SPEECH AND LANGUAGE DISORDER

    http://iris.ucl.ac.uk/iris/publication/195847/3

  4. Emergence of cognitive, language and motor impairment associated with the mutation of the...

    http://iris.ucl.ac.uk/iris/publication/1212009/1

  5. IRIS profile Faraneh Vargha-Khadem | UCL Great Ormond Street...

    Another area of research interest concerns the speech and language disorder associated with the FOXP2 gene mutation. ... Through the study of the three-generational KE family, we have identified the phenotype of verbal and orofacial dyspraxia resulting

    https://www.ucl.ac.uk/child-health/people/iris-profile-faraneh-vargha-khadem

  6. The speech gene FOXP2 is not imprinted.

    http://iris.ucl.ac.uk/iris/publication/787701/2

  7. The speech gene FOXP2 is not imprinted

    http://iris.ucl.ac.uk/iris/publication/838203/7

  8. Early neuroimaging markers of FOXP2 intragenic deletion.

    FOXP2 is the major gene associated with severe, persistent, developmental speech and language disorders. While studies in the original family in which a FOXP2 mutation was found showed volume reduction and reduced activation in core language and

    http://iris.ucl.ac.uk/iris/publication/1184433/1

  9. Identification of foxp2 truncation as a novel cause of developmental speech disorder

    http://iris.ucl.ac.uk/iris/publication/53645/1

  10. FOXP2 and the neuroanatomy of speech and language.

    That speech and language are innate capacities of the human brain has long been widely accepted, but only recently has an entry point into the genetic basis of these remarkable faculties been found. The discovery of a mutation in FOXP2 in a family

    http://iris.ucl.ac.uk/iris/publication/168251/2

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