Rare mutations of the FOXP2 transcription factor gene cause a monogenic syndrome
characterized by impaired speech development and linguistic deficits. Recent genomic …

… in these inherited forms of speech and language disorder. Thus, we … molecules, neurons
and the brain, which will provide a new understanding of the aetiology of speech and language …

… The molecular mapping data thus provided experimental confirmation that the speech and
language problems of the family had a genetic origin and localized the responsible gene to a …

… basis of human speech and language is being transformed by developments in molecular
… on the genetic architecture underlying language-related disorders (speech apraxia, specific …

… molecular basis of this remarkable suite of abilities, catalysed by successful genomic studies
of developmental speech and language … difficulties in language, speech or reading. Such …

… Genetic factors associated with language contribute to various molecular, cellular and …
great complexity of the speech and language process[6]. Also, language disabilities in children …

… In this article, we provide a critical review of the literature on speech … a window to understanding
how the notion of critical periods might apply to the acquisition of one part of language: …

Human speech, language, and cognition derive from anatomy and neural mechanisms that
have been shaped by the Darwinian process of natural selection acting on variation but that …

… Specifically, we argue that the FoxP2 transcription factor and the regulatory molecular … ‘speech’
aspects of language, whereas syntax and particularly semantics, the language domains …

… to different aspects of speech and language difficulties. In … , speech-sound disorder (SSD),
specific language impairment (… of the etiology of speech and language disorders and enable …