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There are 63259 results for: content related to: Defining the autism minimum candidate gene region on chromosome 7

  1. 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

  2. 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

  3. Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31

    American Journal of Medical Genetics

    Volume 96, Issue 2, 3 April 2000, Pages: 228–234, Pamela Warburton, Gillian Baird, Wai Chen, Kathleen Morris, Brian W. Jacobs, Shirley Hodgson and Zoe Docherty

    Version of Record online : 13 APR 2000, DOI: 10.1002/(SICI)1096-8628(20000403)96:2<228::AID-AJMG20>3.0.CO;2-G

  4. Incorporating language phenotypes strengthens evidence of linkage to autism

    American Journal of Medical Genetics

    Volume 105, Issue 6, 8 August 2001, Pages: 539–547, Yuki Bradford, Jonathan Haines, Holli Hutcheson, Marybeth Gardiner, Terry Braun, Val Sheffield, Tom Cassavant, Wen Huang, Kai Wang, Veronica Vieland, Susan Folstein, Susan Santangelo and Joseph Piven

    Version of Record online : 6 JUL 2001, DOI: 10.1002/ajmg.1497

  5. Autism spectrum disorders: Molecular genetic advances

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

    Volume 142C, Issue 1, 15 February 2006, Pages: 13–23, Elena Bacchelli and Elena Maestrini

    Version of Record online : 17 JAN 2006, DOI: 10.1002/ajmg.c.30078

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    Bioinformatic analysis of autism positional candidate genes using biological databases and computational gene network prediction

    Genes, Brain and Behavior

    Volume 2, Issue 5, October 2003, Pages: 303–320, A. L. Yonan, A. A. Palmer, K. C. Smith, I. Feldman, H. K. Lee, J. M. Yonan, S. G. Fischer, P. Pavlidis and T. C. Gilliam

    Version of Record online : 16 OCT 2003, DOI: 10.1034/j.1601-183X.2003.00041.x

  7. Genomic screen and follow-up analysis for autistic disorder

    American Journal of Medical Genetics

    Volume 114, Issue 1, 8 January 2002, Pages: 99–105, Yujun Shao, Chantelle M. Wolpert, Kimberly L. Raiford, Marisa M. Menold, Shannon L. Donnelly, Sarah A. Ravan, Meredyth P. Bass, Cate McClain, Lennart von Wendt, Jeffery M. Vance, Ruth H. Abramson, Harry H. Wright, Allison Ashley-Koch, John R. Gilbert, Robert G. DeLong, Michael L. Cuccaro and Margaret A. Pericak-Vance

    Version of Record online : 5 DEC 2001, DOI: 10.1002/ajmg.10153

  8. 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

  9. A balanced reciprocal translocation t(5;7)(q14;q32) associated with autistic disorder: Molecular analysis of the chromosome 7 breakpoint

    American Journal of Medical Genetics

    Volume 105, Issue 8, 8 December 2001, Pages: 729–736, Dmitry Tentler, Göran Brandberg, Catalina Betancur, Christopher Gillberg, Göran Annerén, Christina Orsmark, Eric D Green, Birgit Carlsson and Niklas Dahl

    Version of Record online : 1 NOV 2001, DOI: 10.1002/ajmg.1607

  10. Evidence supporting WNT2 as an autism susceptibility gene

    American Journal of Medical Genetics

    Volume 105, Issue 5, 8 July 2001, Pages: 406–413, Thomas H. Wassink, Joseph Piven, Veronica J. Vieland, Jian Huang, Ruth E. Swiderski, Jennifer Pietila, Terry Braun, Gretel Beck, Susan E. Folstein, Jonathon L. Haines and Val C. Sheffield

    Version of Record online : 17 MAY 2001, DOI: 10.1002/ajmg.1401

  11. Genetic Influences and Autism

    Handbook of Autism and Pervasive Developmental Disorders, Volume 1, Third Edition

    Fred R. Volkmar, Rhea Paul, Ami Klin, Donald Cohen, Pages: 425–452, 2013

    Published Online : 30 SEP 2013, DOI: 10.1002/9780470939345.ch16

  12. Toward a developmental neurobiology of autism

    Mental Retardation and Developmental Disabilities Research Reviews

    Volume 10, Issue 4, November 2004, Pages: 303–317, Franck Polleux and Jean M. Lauder

    Version of Record online : 21 JAN 2005, DOI: 10.1002/mrdd.20044

  13. Syndromes and epistemology II: Is autism a polygenic disorder?

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 17, 1 September 2008, Pages: 2203–2212, Gene S. Fisch

    Version of Record online : 29 JUL 2008, DOI: 10.1002/ajmg.a.32438

  14. Childhood-onset schizophrenia/autistic disorder and t(1;7) reciprocal translocation: Identification of a BAC contig spanning the translocation breakpoint at 7q21

    American Journal of Medical Genetics

    Volume 96, Issue 6, 4 December 2000, Pages: 749–753, WenLiang Yan, Xin-Yuan Guan, Eric D. Green, Rob Nicolson, Tieng K. Yap, Jinghui Zhang, Leslie K. Jacobsen, Donna M. Krasnewich, Sanjiv Kumra, Marge C. Lenane, Peter Gochman, Patricia J. Damschroder-Williams, Lisa E. Esterling, Robert T. Long, Brian M. Martin, Ellen Sidransky, Judith L. Rapoport and Edward I. Ginns

    Version of Record online : 14 DEC 2000, DOI: 10.1002/1096-8628(20001204)96:6<749::AID-AJMG10>3.0.CO;2-K

  15. Examination of candidate genes in language disorder: A model of genetic association for treatment studies

    Mental Retardation and Developmental Disabilities Research Reviews

    Volume 10, Issue 3, August 2004, Pages: 208–217, Jonathan Haines and Stephen Camarata

    Version of Record online : 20 DEC 2004, DOI: 10.1002/mrdd.20035

  16. An autosomal genomic screen for autism

    American Journal of Medical Genetics

    Volume 88, Issue 6, 15 December 1999, Pages: 609–615,

    Version of Record online : 20 APR 2000, DOI: 10.1002/(SICI)1096-8628(19991215)88:6<609::AID-AJMG7>3.0.CO;2-L

  17. The search for autism disease genes

    Mental Retardation and Developmental Disabilities Research Reviews

    Volume 10, Issue 4, November 2004, Pages: 272–283, Thomas H Wassink, Linda M Brzustowicz, Christopher W Bartlett and Peter Szatmari

    Version of Record online : 21 JAN 2005, DOI: 10.1002/mrdd.20041

  18. 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

  19. 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

  20. HotSpots

    Clinical Genetics

    Volume 61, Issue 1, January 2002, Pages: 7–12, ME Suzanne Lewis

    Version of Record online : 19 MAR 2002, DOI: 10.1034/j.1399-0004.2002.610102.x