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Deep phenotyping of speech and language skills in individuals with 16p11.2 deletion
High penetration children speech apraxia prevalence oral exercise
2018/3/5
Advance online publication. doi:10.1038/s41431-018-0102-x.
Recurrent deletions of a ~600-kb region of 16p11.2 have been associated with a highly penetrant form of childhood apraxia of speech (CAS). Y...
Investigation of the biological basis of human speech and language is being transformed by developments in molecular technologies, including high-throughput genotyping and next-generation sequencing o...
Language is not isolated from its wider environment: Vocal tract influences on the evolution of speech and language
Biases Language change Linguistic diversity
2017/8/25
Language is not a purely cultural phenomenon somehow isolated from its wider environment, and we may only understand its origins and evolution by seriously considering its embedding in this environmen...
A de novo FOXP1 variant in a patient with autism, intellectual disability and severe speech and language impairment
autism intellectual disability
2015/12/18
FOXP1 (forkhead box protein P1; OMIM 605515) belongs to the FOX
gene family of transcription factor proteins, defined by the presence of
a characteristic DNA-binding domain known as the forkhe...
On the relationship of speech to language.