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There are 9852 results for: content related to: ORIGINAL ARTICLE: Genomic sister-disorders of neurodevelopment: an evolutionary approach

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    A functional network module for Smith–Magenis syndrome

    Clinical Genetics

    Volume 75, Issue 4, April 2009, Pages: 364–374, S Girirajan, HT Truong, CL Blanchard and SH Elsea

    Version of Record online : 19 FEB 2009, DOI: 10.1111/j.1399-0004.2008.01135.x

  2. RAI1 point mutations, CAG repeat variation, and SNP analysis in non-deletion Smith–Magenis syndrome

    American Journal of Medical Genetics Part A

    Volume 140A, Issue 22, 15 November 2006, Pages: 2454–2463, Weimin Bi, G. Mustafa Saifi, Santhosh Girirajan, Xin Shi, Barbara Szomju, Helen Firth, R. Ellen Magenis, Lorraine Potocki, Sarah H. Elsea and James R. Lupski

    Version of Record online : 13 OCT 2006, DOI: 10.1002/ajmg.a.31510

  3. Native pancreatic α-cell adaptation in streptozotocin-induced diabetic primates: importance for pig islet xenotransplantation

    Xenotransplantation

    Volume 16, Issue 3, May/June 2009, Pages: 152–163, Denis Dufrane, Jean-François Maillart, Najima Aouassar, Rose-Marie Goebbels, Yves Guiot and Pierre Gianello

    Version of Record online : 25 JUN 2009, DOI: 10.1111/j.1399-3089.2009.00530.x

  4. Smith–Magenis syndrome and moyamoya disease in a patient with del(17)(p11.2p13.1)

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 9, 1 May 2007, Pages: 999–1008, Santhosh Girirajan, Roberto Mendoza-Londono, Christopher N. Vlangos, Lucie Dupuis, Norma J. Nowak, David J. Bunyan, Eli Hatchwell and Sarah H. Elsea

    Version of Record online : 12 APR 2007, DOI: 10.1002/ajmg.a.31689

  5. Diagnostic FISH probes for del(17)(p11.2p11.2) associated with Smith–Magenis syndrome should contain the RAI1 gene

    American Journal of Medical Genetics Part A

    Volume 132A, Issue 3, 30 January 2005, Pages: 278–282, Christopher N. Vlangos, Meredith Wilson, Jan Blancato, Ann C.M. Smith and Sarah H. Elsea

    Version of Record online : 7 DEC 2004, DOI: 10.1002/ajmg.a.30461

  6. Common Vehicles for Nonclinical Evaluation of Therapeutic Agents

    Standard Article

    Pharmaceutical Sciences Encyclopedia

    Published Online : 15 MAR 2010, DOI: 10.1002/9780470571224.pse158

  7. Circadian abnormalities in mouse models of smith–magenis syndrome: Evidence for involvement of RAI1

    American Journal of Medical Genetics Part A

    Volume 161, Issue 7, July 2013, Pages: 1561–1568, Melanie Lacaria, Wenli Gu and James R Lupski

    Version of Record online : 23 MAY 2013, DOI: 10.1002/ajmg.a.35941

  8. Ontogenetic correlates of diet in Malagasy lemurs

    American Journal of Physical Anthropology

    Volume 123, Issue 3, March 2004, Pages: 250–276, L.R. Godfrey, K.E. Samonds, W.L. Jungers, M.R. Sutherland and M.T. Irwin

    Version of Record online : 7 JUL 2003, DOI: 10.1002/ajpa.10315

  9. Smith–Magenis Syndrome

    Standard Article

    eLS

    Sarah H Elsea and Brenda Finucane

    Published Online : 15 MAR 2009, DOI: 10.1002/9780470015902.a0021428

  10. HER2 FISH results in breast cancers with increased CEN17 signals using alternative chromosome 17 probes – reclassifying cases in the equivocal category

    Histopathology

    Volume 71, Issue 4, October 2017, Pages: 610–625, Maria-Anna Holzschuh, Zbigniew Czyz, Sven Hauke, Elisabeth C Inwald, Bernhard Polzer and Gero Brockhoff

    Version of Record online : 6 JUL 2017, DOI: 10.1111/his.13253

  11. Gender, genotype, and phenotype differences in Smith–Magenis syndrome: a meta-analysis of 105 cases

    Clinical Genetics

    Volume 71, Issue 6, June 2007, Pages: 540–550, EA Edelman, S Girirajan, B Finucane, PI Patel, JR Lupski, ACM Smith and SH Elsea

    Version of Record online : 18 MAY 2007, DOI: 10.1111/j.1399-0004.2007.00815.x

  12. Models of Primate Evolution

    Standard Article

    eLS

    Ken Sayers

    Published Online : 16 NOV 2015, DOI: 10.1002/9780470015902.a0026406

  13. First evidence of Smith–Magenis syndrome in mother and daughter due to a novel RAI mutation

    American Journal of Medical Genetics Part A

    Volume 173, Issue 1, January 2017, Pages: 231–238, Fabio Acquaviva, Maria Elena Sana, Matteo Della Monica, Michele Pinelli, Diana Postorivo, Paolo Fontana, Maria Teresa Falco, Anna Maria Nardone, Fortunato Lonardo, Maria Iascone and Gioacchino Scarano

    Version of Record online : 28 SEP 2016, DOI: 10.1002/ajmg.a.37989

  14. Autism spectrum disorders: The quest for genetic syndromes

    American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

    Volume 162, Issue 4, June 2013, Pages: 327–366, Dimitrios I. Zafeiriou, Athina Ververi, Vaios Dafoulis, Efrosini Kalyva and Euthymia Vargiami

    Version of Record online : 3 MAY 2013, DOI: 10.1002/ajmg.b.32152

  15. Ionotropic glutamate receptors: Which ones, when, and where in the mammalian neocortex

    Journal of Comparative Neurology

    Volume 525, Issue 4, March 1, 2017, Pages: 976–1033, Minela Hadzic, Alexander Jack and Petra Wahle

    Version of Record online : 27 SEP 2016, DOI: 10.1002/cne.24103

  16. TOWARDS A THEORETICAL EXPLORATION OF THE DIFFERENTIAL URBANISATION MODEL IN SUB-SAHARAN AFRICA: THE BOTSWANA CASE

    Tijdschrift voor economische en sociale geografie

    Volume 97, Issue 4, September 2006, Pages: 418–433, THANDO D. GWEBU

    Version of Record online : 31 OCT 2006, DOI: 10.1111/j.1467-9663.2006.00346.x

  17. Absolute abundances and affinity states of dopamine receptors in mammalian brain: A review

    Synapse

    Volume 65, Issue 9, September 2011, Pages: 892–909, Paul Cumming

    Version of Record online : 7 APR 2011, DOI: 10.1002/syn.20916

  18. Evaluation of a test for its suitability in the diagnosis of variant Creutzfeldt–Jakob disease

    Vox Sanguinis

    Volume 105, Issue 3, October 2013, Pages: 196–204, J. K. Cooper, N. Andrews, K. Ladhani, E. Bujaki and P. D. Minor

    Version of Record online : 16 JUN 2013, DOI: 10.1111/vox.12037

  19. Delayed diagnosis in a house of correction: Smith–Magenis syndrome due to a de novo nonsense RAI1 variant

    American Journal of Medical Genetics Part A

    Volume 170, Issue 9, September 2016, Pages: 2383–2388, Patra Yeetong, Thierry Vilboux, Carla Ciccone, Kristin Boulier, Rhonda E. Schnur, William A. Gahl, Marjan Huizing, Gonzalo Laje and Ann C. M. Smith

    Version of Record online : 17 JUN 2016, DOI: 10.1002/ajmg.a.37602

  20. Duplication of 17(p11.2p11.2) in a male child with autism and severe language delay

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 5, 1 March 2008, Pages: 636–643, Alisa Nakamine, Leonid Ouchanov, Patricia Jiménez, Elina R. Manghi, Marcela Esquivel, Silvia Monge, Marietha Fallas, Barbara K. Burton, Barbara Szomju, Sarah H. Elsea, Christian R. Marshall, Stephen W. Scherer and L. Alison McInnes

    Version of Record online : 2 MAR 2007, DOI: 10.1002/ajmg.a.31636