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There are 44343 results for: content related to: Agenesis of the corpus callosum in California 1983–2003: A population-based study

  1. Agenesis and dysgenesis of the corpus callosum: Clinical, genetic and neuroimaging findings in a series of 41 patients

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 19, 1 October 2008, Pages: 2501–2511, Chayim Can Schell-Apacik, Kristina Wagner, Moritz Bihler, Birgit Ertl-Wagner, Uwe Heinrich, Eva Klopocki, Vera M. Kalscheuer, Maximilian Muenke and Hubertus von Voss

    Article first published online : 15 SEP 2008, DOI: 10.1002/ajmg.a.32476

  2. Genetic and functional analyses identify DISC1 as a novel callosal agenesis candidate gene

    American Journal of Medical Genetics Part A

    Volume 155, Issue 8, August 2011, Pages: 1865–1876, Nathan Osbun, Jiang Li, Mary C. O'Driscoll, Zoe Strominger, Mari Wakahiro, Eric Rider, Polina Bukshpun, Elena Boland, Cailyn H. Spurrell, Wendy Schackwitz, Len A. Pennacchio, William B. Dobyns, Graeme C.M. Black and Elliott H. Sherr

    Article first published online : 7 JUL 2011, DOI: 10.1002/ajmg.a.34081

  3. Identification of genomic loci contributing to agenesis of the corpus callosum

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 9, September 2010, Pages: 2145–2159, Mary C. O'Driscoll, Graeme C. M. Black, Jill Clayton-Smith, Elliott H. Sherr and William B. Dobyns

    Article first published online : 3 AUG 2010, DOI: 10.1002/ajmg.a.33558

  4. Vici syndrome associated with sensorineural hearing loss and evidence of neuromuscular involvement on muscle biopsy

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 3, March 2010, Pages: 741–747, Verity McClelland, Thomas Cullup, Istvan Bodi, Deborah Ruddy, Anna Buj-Bello, Valerie Biancalana, J. Boehm, Marc Bitoun, Owen Miller, Wajanat Jan, Esse Menson, Luis Amaya, John Trounce, Jocelyn Laporte, Shehla Mohammed, Caroline Sewry, Julian Raiman and Heinz Jungbluth

    Article first published online : 22 FEB 2010, DOI: 10.1002/ajmg.a.33296

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    Phenotype and natural history in Marshall–Smith syndrome

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 11, November 2010, Pages: 2714–2726, Adam C. Shaw, Inge D.C. van Balkom, Mislen Bauer, Trevor R.P. Cole, Marie-Ange Delrue, Arie Van Haeringen, Eva Holmberg, Samantha J.L. Knight, Geert Mortier, Sheela Nampoothiri, Silvija Pušeljić, Martin Zenker, Valerie Cormier-Daire and Raoul C.M. Hennekam

    Article first published online : 14 OCT 2010, DOI: 10.1002/ajmg.a.33709

  6. Neuroimaging aspects of Aicardi syndrome

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 22, 15 November 2008, Pages: 2871–2878, Bobbi Hopkins, V. Reid Sutton, Richard Alan Lewis, Ignatia Van den Veyver and Gary Clark

    Article first published online : 16 OCT 2008, DOI: 10.1002/ajmg.a.32537

  7. Molecular and electronic structures of endohedral fullerenes, Sc2C2@C3v–C82 and Sc2@C3v–C82: Benchmark for SCC-DFTB and proposal of new inner cluster structures

    physica status solidi (b)

    Volume 249, Issue 2, February 2012, Pages: 324–334, Yoshio Nishimoto, Zhi Wang, Keiji Morokuma and Stephan Irle

    Article first published online : 19 JAN 2012, DOI: 10.1002/pssb.201100767

  8. Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 5, May 2012, Pages: 1233–1235, Lucilene Arilho Ribeiro-Bicudo, Rodrigo G. Quiezi, Maria Leine Guion-Almeida, Chiara Legnaro and Antonio Richieri-Costa

    Article first published online : 11 APR 2012, DOI: 10.1002/ajmg.a.35305

  9. Atypical findings in three patients with Pai syndrome and literature review

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 11, November 2012, Pages: 2899–2904, Damien Lederer, Brian Wilson, Pierre Lefesvre, Vincent Vander Poorten, Nigel Kirkham, Dipayan Mitra, Christine Verellen-Dumoulin and Koenraad Devriendt

    Article first published online : 17 SEP 2012, DOI: 10.1002/ajmg.a.35592

  10. Visual aesthetics in store environment and its moderating role on consumer intention

    Journal of Consumer Behaviour

    Volume 9, Issue 5, September/October 2010, Pages: 364–380, Valter Afonso Vieira

    Article first published online : 28 SEP 2010, DOI: 10.1002/cb.324

  11. High prevalence of orofacial clefts in Shanxi Province in northern China, 2003–2004

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 20, 15 October 2008, Pages: 2637–2643, Zhiwen Li, Aiguo Ren, Jianmeng Liu, Le Zhang, Rongwei Ye, Song Li and Zhu Li

    Article first published online : 16 SEP 2008, DOI: 10.1002/ajmg.a.32492

  12. Subtypes of frontonasal dysplasia are useful in determining clinical prognosis

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 24, 15 December 2007, Pages: 3069–3078, E. Wu, K. Vargevik and A.M. Slavotinek

    Article first published online : 22 OCT 2007, DOI: 10.1002/ajmg.a.31963

  13. Cerebro-oculo-nasal syndrome: 13 new Brazilian cases

    American Journal of Medical Genetics Part A

    Volume 143A, Issue 24, 15 December 2007, Pages: 3252–3266, Maria Leine Guion-Almeida, Roseli Maria Zechi-Ceide and Antonio Richieri-Costa

    Article first published online : 5 NOV 2007, DOI: 10.1002/ajmg.a.32090

  14. Genotype–phenotype correlations in Rubinstein–Taybi syndrome

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 19, 1 October 2008, Pages: 2512–2519, E.K. Schorry, M. Keddache, N. Lanphear, J.H. Rubinstein, S. Srodulski, D. Fletcher, R.I. Blough-Pfau and G.A. Grabowski

    Article first published online : 15 SEP 2008, DOI: 10.1002/ajmg.a.32424

  15. Mental health and quality of life after genetic testing for Huntington disease: A long-term effect study in Germany

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 16, 15 August 2008, Pages: 2078–2085, Claudia Licklederer, Gerhard Wolff and Jürgen Barth

    Article first published online : 14 JUL 2008, DOI: 10.1002/ajmg.a.32423

  16. Clinical and molecular cytogenetic characterization of four patients with unbalanced translocation der(1)t(1;22)(p36;q13)

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 21, 1 November 2008, Pages: 2777–2784, Marzena Gajecka, Reem Saadeh, Katherine L. Mackay, Caron D. Glotzbach, Krystyna Spodar, David Chitayat and Lisa G. Shaffer

    Article first published online : 27 OCT 2008, DOI: 10.1002/ajmg.a.32427

  17. Fear of health insurance loss among individuals at risk for Huntington disease

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 16, 15 August 2008, Pages: 2070–2077, Emily Oster, E. Ray Dorsey, Jan Bausch, Aileen Shinaman, Elise Kayson, David Oakes, Ira Shoulson and Kimberly Quaid

    Article first published online : 14 JUL 2008, DOI: 10.1002/ajmg.a.32422

  18. DTI at long diffusion time improves fiber tracking

    NMR in Biomedicine

    Volume 23, Issue 5, June 2010, Pages: 459–465, Swati Rane, Govind Nair and Timothy Q. Duong

    Article first published online : 19 FEB 2010, DOI: 10.1002/nbm.1482

  19. Health-related issues in individuals with agenesis of the corpus callosum

    Child: Care, Health and Development

    Volume 32, Issue 3, May 2006, Pages: 333–342, D. Doherty, S. Tu, K. Schilmoeller and G. Schilmoeller

    Article first published online : 29 MAR 2006, DOI: 10.1111/j.1365-2214.2006.00602.x

  20. Radiological evolution in IMAGe association: A case report

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 16, 15 August 2008, Pages: 2130–2133, Naoko Amano, Hori Naoaki, Tomohiro Ishii, Satoshi Narumi, Rumi Hachiya, Gen Nishimura and Tomonobu Hasegawa

    Article first published online : 14 JUL 2008, DOI: 10.1002/ajmg.a.32425