Search research articles
Contact Us
Filters
Showing results (31-40 of 56) with videos related to
Page
of 6
Sort By:
Journal of Speech, Language, and Hearing Research : JSLHR
|
December 28, 2005
Toward diagnostic and phenotype markers for genetically transmitted speech delay
Lawrence 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 hybridization
Jennifer 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 FOXP2
Lawrence 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 FOXP2
J 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 children
Jennell 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 study
Barbara 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 language
Barbara 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 disorders
Erin 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 syndrome
Gordana Raca, Becky S Baas, Salman Kirmani, et al.
Page
of 6
Search research articles
Search
Showing results (31-40 of 56) with videos related to
Sort By:
Page
of 6
Journal of Speech, Language, and Hearing Research : JSLHR
|
December 28, 2005
Toward diagnostic and phenotype markers for genetically transmitted speech delay
Lawrence 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 hybridization
Jennifer 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 FOXP2
Lawrence 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 FOXP2
J 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 children
Jennell 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 study
Barbara 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 language
Barbara 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 disorders
Erin 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 syndrome
Gordana Raca, Becky S Baas, Salman Kirmani, et al.
Page
of 6