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Lawrence D Shriberg

Showing results (31-40 of 56) with videos related to

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Journal of Speech, Language, and Hearing Research : JSLHR|December 28, 2005
Toward diagnostic and phenotype markers for genetically transmitted speech delayLawrence D Shriberg, Barbara A Lewis, J Bruce Tomblin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 7, 2012
Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridizationJennifer J S Laffin, Gordana Raca, Craig A Jackson, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|June 22, 2006
Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2Lawrence D Shriberg, Kirrie J Ballard, J Bruce Tomblin, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|July 29, 2009
A nonword repetition task for speakers with misarticulations: the Syllable Repetition Task (SRT)Lawrence D Shriberg, Heather L Lohmeier, Thomas F Campbell, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|October 3, 2009
Language features in a mother and daughter of a chromosome 7;13 translocation involving FOXP2J Bruce Tomblin, Marlea O'Brien, Lawrence D Shriberg, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|July 31, 2014
Data-driven subclassification of speech sound disorders in preschool childrenJennell C Vick, Thomas F Campbell, Lawrence D Shriberg, et al.
Journal of Communication Disorders|January 3, 2006
Dimensions of early speech sound disorders: A factor analytic studyBarbara A Lewis, Lisa A Freebairn, Amy J Hansen, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|January 2, 2007
The genetic bases of speech sound disorders: evidence from spoken and written languageBarbara A Lewis, Lawrence D Shriberg, Lisa A Freebairn, et al.
Brain Research|December 8, 2014
Functional MRI evidence for fine motor praxis dysfunction in children with persistent speech disordersErin Redle, Jennifer Vannest, Thomas Maloney, et al.
European Journal of Human Genetics : EJHG|August 23, 2012
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndromeGordana Raca, Becky S Baas, Salman Kirmani, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

Sort By:
Pageof 6
Journal of Speech, Language, and Hearing Research : JSLHR|December 28, 2005
Toward diagnostic and phenotype markers for genetically transmitted speech delayLawrence D Shriberg, Barbara A Lewis, J Bruce Tomblin, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 7, 2012
Novel candidate genes and regions for childhood apraxia of speech identified by array comparative genomic hybridizationJennifer J S Laffin, Gordana Raca, Craig A Jackson, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|June 22, 2006
Speech, prosody, and voice characteristics of a mother and daughter with a 7;13 translocation affecting FOXP2Lawrence D Shriberg, Kirrie J Ballard, J Bruce Tomblin, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|July 29, 2009
A nonword repetition task for speakers with misarticulations: the Syllable Repetition Task (SRT)Lawrence D Shriberg, Heather L Lohmeier, Thomas F Campbell, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|October 3, 2009
Language features in a mother and daughter of a chromosome 7;13 translocation involving FOXP2J Bruce Tomblin, Marlea O'Brien, Lawrence D Shriberg, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|July 31, 2014
Data-driven subclassification of speech sound disorders in preschool childrenJennell C Vick, Thomas F Campbell, Lawrence D Shriberg, et al.
Journal of Communication Disorders|January 3, 2006
Dimensions of early speech sound disorders: A factor analytic studyBarbara A Lewis, Lisa A Freebairn, Amy J Hansen, et al.
Journal of Speech, Language, and Hearing Research : JSLHR|January 2, 2007
The genetic bases of speech sound disorders: evidence from spoken and written languageBarbara A Lewis, Lawrence D Shriberg, Lisa A Freebairn, et al.
Brain Research|December 8, 2014
Functional MRI evidence for fine motor praxis dysfunction in children with persistent speech disordersErin Redle, Jennifer Vannest, Thomas Maloney, et al.
European Journal of Human Genetics : EJHG|August 23, 2012
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndromeGordana Raca, Becky S Baas, Salman Kirmani, et al.
Pageof 6