Feature-blind grammar and dysphasia

@article{Gopnik1990FeatureblindGA,
  title={Feature-blind grammar and dysphasia},
  author={Myrna Gopnik},
  journal={Nature},
  year={1990},
  volume={344},
  pages={715-715}
}
  • M. Gopnik
  • Published 19 April 1990
  • Psychology, Medicine
  • Nature

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...

References

SHOWING 1-2 OF 2 REFERENCES

The Assessment of Bilingual Aphasia

The Bilingual Aphasia Test is a comprehensive language test designed to assess the differential loss or sparing of various language functions in previously bilingual individuals. The individual is

The grammatical characterization of developmental dysphasia

This paper deals with child-language-acquisition disorders in the area of grammar, and it presents some of the results from our research study on developmental dysphasia in German children. An