Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2.

@article{Shriberg2006SpeechPA,
  title={Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2.},
  author={L. Shriberg and K. Ballard and J. Tomblin and J. Duffy and K. Odell and C. A. Williams},
  journal={Journal of speech, language, and hearing research : JSLHR},
  year={2006},
  volume={49 3},
  pages={
          500-25
        }
}
  • L. Shriberg, K. Ballard, +3 authors C. A. Williams
  • Published 2006
  • Medicine, Psychology
  • Journal of speech, language, and hearing research : JSLHR
  • 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 of the widely cited KE family, whose communicative disorders have been associated with a point mutation in the FOXP2 gene, both mother and daughter had cognitive, language, and speech challenges. A… CONTINUE READING
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