Results 1 -
4
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4
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Dyspraxia
- ... syndrome (ECSWS), autosomal dominant rolandic epilepsy with speech dyspraxia (ADRESD), intermediate epilepsy-aphasia disorder (IEAD), atypical childhood ...
- ... genetic change. Speech and language disorder with orofacial dyspraxia Speech-language disorder 1 Genetic Testing Registry: Childhood ... a paternally inherited FOXP2 gene in developmental verbal dyspraxia. Am J Hum Genet. 2006 Nov;79(5): ...
- ... Scherer SW. Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2. ...
- ... a paternally inherited FOXP2 gene in developmental verbal dyspraxia. Am J Hum Genet. 2006 Nov;79(5): ...