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Angela T Morgan

Showing results (91-100 of 148) with videos related to

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European Journal of Human Genetics : EJHG|February 16, 2018
Deep phenotyping of speech and language skills in individuals with 16p11.2 deletionCristina Mei, Evelina Fedorenko, David J Amor, et al.
Scientific Reports|October 14, 2016
Early neuroimaging markers of FOXP2 intragenic deletionFrédérique J Liégeois, Michael S Hildebrand, Alexandra Bonthrone, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthriaSamantha J Turner, Michael S Hildebrand, Susan Block, et al.
Neurology|February 16, 2021
Speech, Language, and Oromotor Skills in Patients With PolymicrogyriaRuth O Braden, Jessica O Boyce, Chloe A Stutterd, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 26, 2018
Characterization of speech and language phenotype in children with NRXN1 deletionsAmanda Brignell, Miya St John, Amber Boys, et al.
Developmental Medicine and Child Neurology|September 21, 2019
Communication in children born very preterm: a prospective cohort studyKatherine Sanchez, Jessica O Boyce, Cristina Mei, et al.
Molecular Autism|December 12, 2025
Atypical GNAO1 variants in severe childhood speech disorders: clinical, genetic, and molecular insightsYonika A Larasati, Moritz Thiel, Ainara Salazar-Villacorta, et al.
European Journal of Human Genetics : EJHG|December 12, 2017
Early speech development in Koolen de Vries syndrome limited by oral praxis and hypotoniaAngela T Morgan, Leenke van Haaften, Karen van Hulst, et al.
Psychiatry Research|November 14, 2025
Combining genetic and behavioral predictors of 11-year language outcomeLoretta Gasparini, Daisy A Shepherd, Katherine Lange, et al.
Developmental Medicine and Child Neurology|January 23, 2025
Adaptive functioning in children and young adults with monogenic neurodevelopmental disordersEmma K Baker, Miya St John, Ruth Braden, et al.
Pageof 15

Showing results (91-100 of 148) with videos related to

Sort By:
Pageof 15
European Journal of Human Genetics : EJHG|February 16, 2018
Deep phenotyping of speech and language skills in individuals with 16p11.2 deletionCristina Mei, Evelina Fedorenko, David J Amor, et al.
Scientific Reports|October 14, 2016
Early neuroimaging markers of FOXP2 intragenic deletionFrédérique J Liégeois, Michael S Hildebrand, Alexandra Bonthrone, et al.
American Journal of Medical Genetics. Part A|August 7, 2013
Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthriaSamantha J Turner, Michael S Hildebrand, Susan Block, et al.
Neurology|February 16, 2021
Speech, Language, and Oromotor Skills in Patients With PolymicrogyriaRuth O Braden, Jessica O Boyce, Chloe A Stutterd, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|October 26, 2018
Characterization of speech and language phenotype in children with NRXN1 deletionsAmanda Brignell, Miya St John, Amber Boys, et al.
Developmental Medicine and Child Neurology|September 21, 2019
Communication in children born very preterm: a prospective cohort studyKatherine Sanchez, Jessica O Boyce, Cristina Mei, et al.
Molecular Autism|December 12, 2025
Atypical GNAO1 variants in severe childhood speech disorders: clinical, genetic, and molecular insightsYonika A Larasati, Moritz Thiel, Ainara Salazar-Villacorta, et al.
European Journal of Human Genetics : EJHG|December 12, 2017
Early speech development in Koolen de Vries syndrome limited by oral praxis and hypotoniaAngela T Morgan, Leenke van Haaften, Karen van Hulst, et al.
Psychiatry Research|November 14, 2025
Combining genetic and behavioral predictors of 11-year language outcomeLoretta Gasparini, Daisy A Shepherd, Katherine Lange, et al.
Developmental Medicine and Child Neurology|January 23, 2025
Adaptive functioning in children and young adults with monogenic neurodevelopmental disordersEmma K Baker, Miya St John, Ruth Braden, et al.
Pageof 15