Speech, Prosody, and Voice Characteristics of a Mother and Daughter With a 7;13 Translocation Affecting FOXP2.

Purpose: The primary goal of this case study was to describe the speech, prosody, and voice characteristics of a mother and daughter with a breakpoint in a balanced 7;13 chromosomal translocation that disrupted the transcription gene, FOXP2 (cf. J. B. Tomblin et al., 2005). As with affected members...

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Publicado en:	Journal of Speech, Language & Hearing Research Vol. 49; no. 3; pp. 500 - 526
Autores principales:	Shriberg, Lawrence D., Ballard, Kirrie J., Tomblin, J. Bruce
Formato:	Artículo
Publicado:	American Speech-Language-Hearing Association June 2006
Materias:	Speech disorders Chromosome abnormalities Rhythm in the English language Genetic disorders
Acceso en línea:	Ver este registro en EBSCOhost