Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia

Míreanna comhchosúla

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