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There are 6080 results for: content related to: NEW APPROACH TO STUDY OF DEVELOPMENTAL DISORDERS PROPOSED

  1. 16p11.2 Deletion Syndrome Mice Display Sensory and Ultrasonic Vocalization Deficits During Social Interactions

    Autism Research

    Volume 8, Issue 5, October 2015, Pages: 507–521, Mu Yang, Elena J. Mahrt, Freeman Lewis, Gillian Foley, Thomas Portmann, Ricardo E. Dolmetsch, Christine V. Portfors and Jacqueline N. Crawley

    Version of Record online : 7 FEB 2015, DOI: 10.1002/aur.1465

  2. You have free access to this content
    Eating in the absence of hunger but not loss of control behaviors are associated with 16p11.2 deletions

    Obesity

    Volume 22, Issue 12, December 2014, Pages: 2625–2631, Richard Gill, Qixuan Chen, Debra D'Angelo and Wendy K. Chung

    Version of Record online : 19 SEP 2014, DOI: 10.1002/oby.20892

  3. Brain MRI abnormalities and spectrum of neurological and clinical findings in three patients with proximal 16p11.2 microduplication

    American Journal of Medical Genetics Part A

    Volume 164, Issue 8, August 2014, Pages: 2003–2012, Isabel Filges, Steven Sparagana, Michael Sargent, Kathryn Selby, Kamilla Schlade-Bartusiak, Gregg T. Lueder, Amy Robichaux-Viehoever, Bradley L. Schlaggar, Joshua S. Shimony and Marwan Shinawi

    Version of Record online : 28 MAY 2014, DOI: 10.1002/ajmg.a.36605

  4. Reciprocal white matter alterations due to 16p11.2 chromosomal deletions versus duplications

    Human Brain Mapping

    Yi Shin Chang, Julia P. Owen, Nicholas J. Pojman, Tony Thieu, Polina Bukshpun, Mari L.J. Wakahiro, Elysa J. Marco, Jeffrey I. Berman, John E. Spiro, Wendy K. Chung, Randy L. Buckner, Timothy P.L. Roberts, Srikantan S. Nagarajan, Elliott H. Sherr and Pratik Mukherjee

    Version of Record online : 24 MAY 2016, DOI: 10.1002/hbm.23211

  5. Scoliosis and vertebral anomalies: Additional abnormal phenotypes associated with chromosome 16p11.2 rearrangement

    American Journal of Medical Genetics Part A

    Volume 164, Issue 5, May 2014, Pages: 1118–1126, Hussam Al-Kateb, Geetika Khanna, Isabel Filges, Natalie Hauser, Dorothy K. Grange, Joseph Shen, Christopher D. Smyser, Shashikant Kulkarni and Marwan Shinawi

    Version of Record online : 23 JAN 2014, DOI: 10.1002/ajmg.a.36401

  6. Microdeletion syndrome 16p11.2-p12.2: Clinical and molecular characterization

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 10, October 2009, Pages: 2106–2112, Maja Hempel, Nuria Rivera Brugués, Janine Wagenstaller, Gaby Lederer, Andrea Weitensteiner, Heide Seidel, Thomas Meitinger and Tim M. Strom

    Version of Record online : 12 AUG 2009, DOI: 10.1002/ajmg.a.33042

  7. Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 156, Issue 2, March 2011, Pages: 225–232, Yiping Shen, Xiaoli Chen, Liwen Wang, Jin Guo, Jianliang Shen, Yu An, Haitao Zhu, Yanli Zhu, Ruolei Xin, Yihua Bao, James F. Gusella, Ting Zhang and Bai-Lin Wu

    Version of Record online : 28 DEC 2010, DOI: 10.1002/ajmg.b.31147

  8. Deletions of 16p11.2 and 19p13.2 in a family with intellectual disability and generalized epilepsy

    American Journal of Medical Genetics Part A

    Volume 161, Issue 7, July 2013, Pages: 1722–1725, Alexander G. Bassuk, Eileen Geraghty, Shu Wu, Saul A. Mullen, Samuel F. Berkovic, Ingrid E. Scheffer and Heather C. Mefford

    Version of Record online : 17 MAY 2013, DOI: 10.1002/ajmg.a.35946

  9. Duplication 16p11.2 in a child with infantile seizure disorder

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 6, June 2010, Pages: 1567–1574, Jirair K. Bedoyan, Ravinesh A. Kumar, Jyotsna Sudi, Faye Silverstein, Todd Ackley, Ramaswamy K. Iyer, Susan L. Christian and Donna M. Martin

    Version of Record online : 14 MAY 2010, DOI: 10.1002/ajmg.a.33415

  10. The atypical 16p11.2 deletion: A not so atypical microdeletion syndrome?

    American Journal of Medical Genetics Part A

    Volume 155, Issue 5, May 2011, Pages: 1066–1072, Daniela Q.C.M. Barge-Schaapveld, Saskia M. Maas, Abeltje Polstra, Lia C. Knegt and Raoul C.M. Hennekam

    Version of Record online : 4 APR 2011, DOI: 10.1002/ajmg.a.33991

  11. The genetic variability and commonality of neurodevelopmental disease

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

    Volume 160C, Issue 2, 15 May 2012, Pages: 118–129, Bradley P. Coe, Santhosh Girirajan and Evan E. Eichler

    Version of Record online : 12 APR 2012, DOI: 10.1002/ajmg.c.31327

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    Structural variation mutagenesis of the human genome: Impact on disease and evolution

    Environmental and Molecular Mutagenesis

    Volume 56, Issue 5, June 2015, Pages: 419–436, James R. Lupski

    Version of Record online : 17 APR 2015, DOI: 10.1002/em.21943

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    Copy-number variation in the pathogenesis of autism spectrum disorder

    Psychiatry and Clinical Neurosciences

    Volume 68, Issue 2, February 2014, Pages: 85–95, Emiko Shishido, Branko Aleksic and Norio Ozaki

    Version of Record online : 29 DEC 2013, DOI: 10.1111/pcn.12128

  14. Association between copy number variants in 16p11.2 and major depressive disorder in a German case–control sample

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 159B, Issue 3, April 2012, Pages: 263–273, Franziska Degenhardt, Lutz Priebe, Stefan Herms, Manuel Mattheisen, Thomas W. Mühleisen, Sandra Meier, Susanne Moebus, Jana Strohmaier, Magdalena Groß, René Breuer, Christoph Lange, Per Hoffmann, Andreas Meyer-Lindenberg, Andreas Heinz, Henrik Walter, Susanne Lucae, Christiane Wolf, Bertram Müller-Myhsok, Florian Holsboer, Wolfgang Maier, Marcella Rietschel, Markus M. Nöthen and Sven Cichon

    Version of Record online : 17 FEB 2012, DOI: 10.1002/ajmg.b.32034

  15. You have full text access to this OnlineOpen article
    Prevalence of selected genomic deletions and duplications in a French–Canadian population-based sample of newborns

    Molecular Genetics & Genomic Medicine

    Volume 1, Issue 2, July 2013, Pages: 87–97, Tracy Tucker, Sylvie Giroux, Valérie Clément, Sylvie Langlois, Jan M. Friedman and François Rousseau

    Version of Record online : 21 MAY 2013, DOI: 10.1002/mgg3.12

  16. Autism spectrum disorder in the genetics clinic: a review

    Clinical Genetics

    Volume 83, Issue 5, May 2013, Pages: 399–407, MT Carter and SW Scherer

    Version of Record online : 21 FEB 2013, DOI: 10.1111/cge.12101

  17. Combined immunodeficiency in a 3-year-old boy with 16p11.2 and 20p12.2-11.2 chromosomal duplications

    American Journal of Medical Genetics Part A

    Volume 164, Issue 2, February 2014, Pages: 535–541, Jacqueline R. Batanian, Stephen R. Braddock, Katherine Christensen and Alan P. Knutsen

    Version of Record online : 5 DEC 2013, DOI: 10.1002/ajmg.a.36305

  18. Dealing with midair collisions in dense collective aerial systems

    Journal of Field Robotics

    Volume 28, Issue 3, May/June 2011, Pages: 405–423, Severin Leven, Jean-Christophe Zufferey and Dario Floreano

    Version of Record online : 23 MAR 2011, DOI: 10.1002/rob.20385

  19. Common recurrent microduplication syndromes: Diagnosis and management in clinical practice

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 5, May 2010, Pages: 1066–1078, Jonathan S. Berg, Lorraine Potocki and Carlos A. Bacino

    Version of Record online : 7 APR 2010, DOI: 10.1002/ajmg.a.33185

  20. The Glycerol-3-Phosphate Acyltransferase TbGAT is Dispensable for Viability and the Synthesis of Glycerolipids in Trypanosoma brucei

    Journal of Eukaryotic Microbiology

    Nipul Patel, Karim A. Pirani, Tongtong Zhu, Melanie Cheung-See-Kit, Sungsu Lee, Daniel G. Chen and Rachel Zufferey

    Version of Record online : 8 MAR 2016, DOI: 10.1111/jeu.12309