Search Results

There are 2085454 results for: content related to: Maternally and paternally inherited deletion of 7q31 involving the FOXP2 gene in two families

  1. Deletion of 7q31.1 supports involvement of FOXP2 in language impairment: Clinical report and review

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 8, 15 April 2007, Pages: 791–798, P.A. Lennon, M.L. Cooper, D.A. Peiffer, K.L. Gunderson, A. Patel, Sarika Peters, S.W. Cheung and C.A. Bacino

    Version of Record online : 1 MAR 2007, DOI: 10.1002/ajmg.a.31632

  2. Speech and language impairment and oromotor dyspraxia due to deletion of 7q31 that involves FOXP2

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 5, 1 March 2006, Pages: 509–514, Susan Zeesman, Małgorzata J.M. Nowaczyk, Ikuko Teshima, Wendy Roberts, Janis Oram Cardy, Jessica Brian, Lili Senman, Lars Feuk, Lucy R. Osborne and Stephen W. Scherer

    Version of Record online : 6 FEB 2006, DOI: 10.1002/ajmg.a.31110

  3. You have full text access to this OnlineOpen article
    FOXP2

    Wiley Interdisciplinary Reviews: Cognitive Science

    Volume 4, Issue 5, September/October 2013, Pages: 547–560, Ron Nudel and Dianne F Newbury

    Version of Record online : 13 AUG 2013, DOI: 10.1002/wcs.1247

  4. Elucidation of a cryptic interstitial 7q31.3 deletion in a patient with a language disorder and mild mental retardation by array-CGH

    American Journal of Medical Genetics Part A

    Volume 129A, Issue 3, 1 September 2004, Pages: 254–260, Christine Tyson, Barbara McGillivray, Chieko Chijiwa and Evica Rajcan-Separovic

    Version of Record online : 21 JUL 2004, DOI: 10.1002/ajmg.a.30245

  5. A de novo interstitial deletion of 7q31.2q31.31 identified in a girl with developmental delay and hearing loss

    American Journal of Medical Genetics Part C: Seminars in Medical Genetics

    Volume 172, Issue 2, June 2016, Pages: 102–108, Jianhua Zhao, Sarah E. Noon, Ian D. Krantz and Yaning Wu

    Version of Record online : 13 APR 2016, DOI: 10.1002/ajmg.c.31488

  6. Mutation screening of FOXP2 in individuals diagnosed with autistic disorder

    American Journal of Medical Genetics Part A

    Volume 118A, Issue 2, 15 April 2003, Pages: 172–175, Julie Gauthier, Ridha Joober, Laurent Mottron, Sandra Laurent, Marketa Fuchs, Violaine De Kimpe and Guy A. Rouleau

    Version of Record online : 17 JAN 2003, DOI: 10.1002/ajmg.a.10105

  7. Phenotype of FOXP2 haploinsufficiency in a mother and son

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 1, January 2012, Pages: 174–181, Gregory M. Rice, Gordana Raca, Kathy J. Jakielski, Jennifer J. Laffin, Christina M. Iyama-Kurtycz, Sigan L. Hartley, Rae E. Sprague, Anne T. Heintzelman and Lawrence D. Shriberg

    Version of Record online : 21 NOV 2011, DOI: 10.1002/ajmg.a.34354

  8. You have free access to this content
    Association between FOXP2 gene and speech sound disorder in Chinese population

    Psychiatry and Clinical Neurosciences

    Volume 64, Issue 5, October 2010, Pages: 565–573, Yunjing Zhao, Hongwei Ma, Yueping Wang, Hong Gao, Chunyan Xi, Tainyi Hua, Yaru Zhao and Guangrong Qiu

    Version of Record online : 28 SEP 2010, DOI: 10.1111/j.1440-1819.2010.02123.x

  9. Association between the FOXP2 gene and autistic disorder in Chinese population

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 127B, Issue 1, 15 May 2004, Pages: 113–116, Xiaohong Gong, Meixiang Jia, Yan Ruan, Mei Shuang, Jing Liu, Suping Wu, Yanqing Guo, Jianzhong Yang, Yansu Ling, Xiaoling Yang and Dai Zhang

    Version of Record online : 13 JAN 2004, DOI: 10.1002/ajmg.b.20162

  10. Genomic imprinting in the development and evolution of psychotic spectrum conditions

    Biological Reviews

    Volume 83, Issue 4, November 2008, Pages: 441–493, Bernard Crespi

    Version of Record online : 9 SEP 2008, DOI: 10.1111/j.1469-185X.2008.00050.x

  11. You have free access to this content
    Differential FoxP2 and FoxP1 expression in a vocal learning nucleus of the developing budgerigar

    Developmental Neurobiology

    Volume 75, Issue 7, July 2015, Pages: 778–790, Osceola Whitney, Tawni Voyles, Erina Hara, Qianqian Chen, Stephanie A. White and Timothy F. Wright

    Version of Record online : 26 NOV 2014, DOI: 10.1002/dneu.22247

  12. Differential coexpression of FoxP1, FoxP2, and FoxP4 in the Zebra Finch (Taeniopygia guttata) song system

    Journal of Comparative Neurology

    Volume 523, Issue 9, 15 June 2015, Pages: 1318–1340, Ezequiel Mendoza, Kirill Tokarev, Daniel N. Düring, Eva Camarillo Retamosa, Michael Weiss, Nshdejan Arpenik and Constance Scharff

    Version of Record online : 2 APR 2015, DOI: 10.1002/cne.23731

  13. You have free access to this content
    Knockdown of FoxP2 alters spine density in Area X of the zebra finch

    Genes, Brain and Behavior

    Volume 9, Issue 7, October 2010, Pages: 732–740, S. B. Schulz, S. Haesler, C. Scharff and C. Rochefort

    Version of Record online : 6 JUL 2010, DOI: 10.1111/j.1601-183X.2010.00607.x

  14. Evaluation of FOXP2 as an autism susceptibility gene

    American Journal of Medical Genetics

    Volume 114, Issue 5, 8 July 2002, Pages: 566–569, Thomas H. Wassink, Joseph Piven, Veronica J. Vieland, Jennifer Pietila, Rhinda J. Goedken, Susan E. Folstein and Val C. Sheffield

    Version of Record online : 8 MAY 2002, DOI: 10.1002/ajmg.10415

  15. A complex chromosome 7q rearrangement identified in a patient with mental retardation, anxiety disorder, and autistic features

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 2, February 2010, Pages: 427–433, Johannes G. Dauwerse, Claudia A. Ruivenkamp, Kerstin Hansson, Godfried M. Marijnissen, Dorien J.M. Peters, Martijn H. Breuning and Yvonne Hilhorst-Hofstee

    Version of Record online : 15 JAN 2010, DOI: 10.1002/ajmg.a.33203

  16. A review of association and linkage studies for genetical analyses of learning disorders

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 144B, Issue 7, 5 October 2007, Pages: 923–943, Emrah Caylak

    Version of Record online : 17 MAY 2007, DOI: 10.1002/ajmg.b.30537

  17. Small intragenic deletion in FOXP2 associated with childhood apraxia of speech and dysarthria

    American Journal of Medical Genetics Part A

    Volume 161, Issue 9, September 2013, Pages: 2321–2326, Samantha J Turner, Michael S. Hildebrand, Susan Block, John Damiano, Michael Fahey, Sheena Reilly, Melanie Bahlo, Ingrid E. Scheffer and Angela T. Morgan

    Version of Record online : 5 AUG 2013, DOI: 10.1002/ajmg.a.36055

  18. You have free access to this content
    Foxp2 regulates neuronal differentiation and neuronal subtype specification

    Developmental Neurobiology

    Volume 74, Issue 7, July 2014, Pages: 723–738, Yi-Chi Chiu, Ming-Yang Li, Yuan-Hsuan Liu, Jing-Ya Ding, Jenn-Yah Yu and Tsu-Wei Wang

    Version of Record online : 18 FEB 2014, DOI: 10.1002/dneu.22166

  19. Chromosome 7

    Standard Article

    eLS

    Stephen W Scherer

    Published Online : 27 JAN 2006, DOI: 10.1038/npg.els.0005816

  20. FoxP2 expression in the cerebellum and inferior olive: Development of the transverse stripe-shaped expression pattern in the mouse cerebellar cortex

    Journal of Comparative Neurology

    Volume 520, Issue 3, 15 February 2012, Pages: 656–677, Hirofumi Fujita and Izumi Sugihara

    Version of Record online : 13 DEC 2011, DOI: 10.1002/cne.22760