Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia

Eitemau Tebyg

• Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia.
  gan: Vernes, S, et al.
  Cyhoeddwyd: (2009)
• Identification of FOXP2 truncation as a novel cause of developmental speech and language deficits.
  gan: MacDermot, K, et al.
  Cyhoeddwyd: (2005)
• Application of psychomotor reeducation method in the treatment of developmental verbal dyspraxia
  gan: Tomić Katarina N., et al.
  Cyhoeddwyd: (2015-01-01)
• Identification of foxp2 truncation as a novel cause of developmental speech disorder.
  gan: MacDermot, K, et al.
  Cyhoeddwyd: (2004)
• Bilateral brain abnormalities associated with dominantly inherited verbal and orofacial dyspraxia.
  gan: Belton, E, et al.
  Cyhoeddwyd: (2003)