Localisation of a gene implicated in a severe speech and language disorder

Author:

Fisher Simon E.,Vargha-Khadem Faraneh,Watkins Kate E.,Monaco Anthony P.,Pembrey Marcus E.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference21 articles.

1. Bishop, D.V.M., North, T. & Donlan, C. Genetic basis of specific language impairment: evidence from a twin study. Dev. Med. Child Neurol. 37, 56–71 (1995).

2. Smith, S.D., Gilger, J.W. & Pennington, B.F. Dyslexia and other specific learning disorders, in Principles and Practice of Medical Genetics (eds. D.L. Rimoin, J.M. Connor & R.E. Pyeritz) 1767–1789 (Churchill Livingston, New York, 1996).

3. Hurst, J.A., Baraitser, M., Auger, E., Graham, F. & Norell, S. An extended family with a dominantly inherited speech disorder. Dev. Med. Child Neurol. 32, 347–355 (1990).

4. Gopnik, M. Feature-blind grammar and dysphasia. Nature 344, 715 (1990).

5. Gopnik, M. & Crago, M.B. Familial aggregation of a developmental language disorder. Cognition 39, 1–50 (1991).

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