Speech, Prosody, and Voice Characteristics of a Mother and Daughter With a 7;13 Translocation Affecting FOXP2
Abstract
Purpose
Method
Results
Conclusion
Get full access to this article
View all available purchase options and get full access to this article.
References
Information & Authors
Information
Published In
Copyright
History
- Received: Mar 24, 2005
- Revised: Jul 13, 2005
- Accepted: Oct 13, 2005
- Published in issue: Jun 1, 2006
Key Words
Authors
Metrics & Citations
Metrics
Article Metrics
View all metricsCitations
If you have the appropriate software installed, you can download article citation data to the citation manager of your choice. Simply select your manager software from the list below and click Download.
For more information or tips please see 'Downloading to a citation manager' in the Help menu.
Citing Literature
- Merve Yazıcı, Çiçek Hocaoğlu, Specific Learning Disorder and Forkhead Box Protein P2 Gene, Handbook of the Biology and Pathology of Mental Disorders, 10.1007/978-3-031-32035-4_101-1, (1-19), (2024).
- Julie Case, Anna Eva Hallin, The Relationship Between Speech Accuracy and Linguistic Measures in Narrative Retells of Children With Speech Sound Disorders, Journal of Speech, Language, and Hearing Research, 10.1044/2023_JSLHR-22-00615, 67, 9S, (3340-3358), (2023).
- Lottie D Morison, Elisabeth Meffert, Miriam Stampfer, Irene Steiner-Wilke, Brigitte Vollmer, Katrin Schulze, Tracy Briggs, Ruth Braden, Adam Vogel, Daisy Thompson-Lake, Chirag Patel, Edward Blair, Himanshu Goel, Samantha Turner, Ute Moog, Angelika Riess, Frederique Liegeois, David A Koolen, David J Amor, Tjitske Kleefstra, Simon E Fisher, Christiane Zweier, Angela T Morgan, In-depth characterisation of a cohort of individuals with missense and loss-of-function variants disrupting FOXP2 , Journal of Medical Genetics, 10.1136/jmg-2022-108734, 60, 6, (597-607), (2022).
- Aiko Iwata‐Otsubo, Victoria H. Klee, Aaliya A. Ahmad, Laurence E. Walsh, Amy M. Breman, A 9.8 Mb deletion at 7q31.2q31.31 downstream of FOXP2 in an individual with speech and language impairment suggests a possible positional effect , Clinical Case Reports, 10.1002/ccr3.6535, 10, 11, (2022).
- Maria Jesus Herrero, Li Wang, David Hernandez-Pineda, Payal Banerjee, Heidi Y. Matos, Meredith Goodrich, Aswini Panigrahi, Nathan Anthony Smith, Joshua G. Corbin, Sex-Specific Social Behavior and Amygdala Proteomic Deficits in Foxp2+/− Mutant Mice, Frontiers in Behavioral Neuroscience, 10.3389/fnbeh.2021.706079, 15, (2021).
- So Hyun Kim, LeeAnne Green‐Snyder, Catherine Lord, Somer Bishop, Kyle J. Steinman, Raphael Bernier, Ellen Hanson, Robin P. Goin‐Kochel, Wendy K. Chung, Language characterization in 16p11.2 deletion and duplication syndromes, American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, 10.1002/ajmg.b.32809, 183, 6, (380-391), (2020).
- Melissa Rieger, Mandy Krumbiegel, Miriam S. Reuter, Anne Schützenberger, André Reis, Christiane Zweier, 7q31.2q31.31 deletion downstream of FOXP2 segregating in a family with speech and language disorder , American Journal of Medical Genetics Part A, 10.1002/ajmg.a.61838, 182, 11, (2737-2741), (2020).
- Raúl Torres-Ruiz, Antonio Benítez-Burraco, Marta Martínez-Lage, Sandra Rodríguez-Perales, Paloma García-Bellido, Functional characterization of two enhancers located downstream FOXP2, BMC Medical Genetics, 10.1186/s12881-019-0810-2, 20, 1, (2019).
- Lawrence D. Shriberg, Edythe A. Strand, Kathy J. Jakielski, Heather L. Mabie, Estimates of the prevalence of speech and motor speech disorders in persons with complex neurodevelopmental disorders, Clinical Linguistics & Phonetics, 10.1080/02699206.2019.1595732, 33, 8, (707-736), (2019).
- Lawrence D. Shriberg, Joan Kwiatkowski, Heather L. Mabie, Estimates of the prevalence of motor speech disorders in children with idiopathic speech delay, Clinical Linguistics & Phonetics, 10.1080/02699206.2019.1595731, 33, 8, (679-706), (2019).
View Options
Sign In Options
ASHA member? If so, log in with your ASHA website credentials for full access.
Member Login