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There are 35249 results for: content related to: Mowat–Wilson syndrome: an underdiagnosed syndrome?

  1. The spectrum of ZEB2 mutations causing the Mowat–Wilson syndrome in Japanese populations

    American Journal of Medical Genetics Part A

    Volume 164, Issue 8, August 2014, Pages: 1899–1908, Yasukazu Yamada, Noriko Nomura, Kenichiro Yamada, Mari Matsuo, Yuka Suzuki, Kiyoko Sameshima, Reiko Kimura, Yuto Yamamoto, Daisuke Fukushi, Yayoi Fukuhara, Naoko Ishihara, Eriko Nishi, George Imataka, Hiroshi Suzumura, Shin-Ichiro Hamano, Kenji Shimizu, Mie Iwakoshi, Kazunori Ohama, Akira Ohta, Hiroyuki Wakamoto, Mitsuharu Kajita, Kiyokuni Miura, Kenji Yokochi, Kenjiro Kosaki, Tatsuo Kuroda, Rika Kosaki, Yoko Hiraki, Kayoko Saito, Seiji Mizuno, Kenji Kurosawa, Nobuhiko Okamoto and Nobuaki Wakamatsu

    Version of Record online : 8 APR 2014, DOI: 10.1002/ajmg.a.36551

    Corrected by:

    Erratum: Erratum to “The spectrum of ZEB2 mutations causing the Mowat-Wilson syndrome in Japanese populations”

    Vol. 167, Issue 6, 1428, Version of Record online: 21 APR 2015

  2. You have free access to this content
    The behavioral phenotype of Mowat–Wilson syndrome

    American Journal of Medical Genetics Part A

    Volume 158A, Issue 2, February 2012, Pages: 358–366, Elizabeth Evans, Stewart Einfeld, David Mowat, John Taffe, Bruce Tonge and Meredith Wilson

    Version of Record online : 13 JAN 2012, DOI: 10.1002/ajmg.a.34405

  3. CHARGE-like presentation, craniosynostosis and mild Mowat–Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases

    American Journal of Medical Genetics Part A

    Volume 164, Issue 10, October 2014, Pages: 2557–2566, Tara L. Wenger, Margaret Harr, Stefania Ricciardi, Elizabeth Bhoj, Avni Santani, Margaret P. Adam, Sarah S. Barnett, Rebecca Ganetzky, Donna M. McDonald-McGinn, Domenica Battaglia, Stefania Bigoni, Angelo Selicorni, Giovanni Sorge, Matteo Della Monica, Francesca Mari, Elena Andreucci, Silvia Romano, Guido Cocchi, Salvatore Savasta, Baris Malbora, Giuseppe Marangi, Livia Garavelli, Marcella Zollino and Elaine H. Zackai

    Version of Record online : 14 AUG 2014, DOI: 10.1002/ajmg.a.36696

  4. Smad-interacting protein 1 affects acute and tonic, but not chronic pain

    European Journal of Pain

    Volume 18, Issue 2, February 2014, Pages: 249–257, B. Pradier, M. Jeub, A. Markert, D. Mauer, K. Tolksdorf, T. Van de Putte, E. Seuntjens, V. Gailus-Durner, H. Fuchs, M. Hrabě de Angelis, D. Huylebroeck, H. Beck, A. Zimmer and I. Rácz

    Version of Record online : 17 JUL 2013, DOI: 10.1002/j.1532-2149.2013.00366.x

  5. Comprehensive ZEB2 gene analysis for Mowat–Wilson syndrome in a North American cohort: A suggested approach to molecular diagnostics

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 11, November 2009, Pages: 2527–2531, Carol J. Saunders, Weiwei Zhao and Holly H. Ardinger

    Version of Record online : 19 OCT 2009, DOI: 10.1002/ajmg.a.33067

  6. Clinical spectrum of eye malformations in four patients with Mowat–Wilson syndrome

    American Journal of Medical Genetics Part A

    Volume 167, Issue 7, July 2015, Pages: 1587–1592, A. Bourchany, I. Giurgea, J. Thevenon, A. Goldenberg, G. Morin, D. Bremond-Gignac, C. Paillot, P. O. Lafontaine, D. Thouvenin, J. Massy, A. Duncombe, C. Thauvin-Robinet, A. Masurel-Paulet, S. El Chehadeh, F. Huet, A. Bron, C. Creuzot-Garcher, S. Lyonnet and L. Faivre

    Version of Record online : 21 APR 2015, DOI: 10.1002/ajmg.a.36898

  7. Mowat–Wilson syndrome: Facial phenotype changing with age: Study of 19 Italian patients and review of the literature

    American Journal of Medical Genetics Part A

    Volume 149A, Issue 3, March 2009, Pages: 417–426, L. Garavelli, M. Zollino, P. Cerruti Mainardi, F. Gurrieri, F. Rivieri, F. Soli, R. Verri, E. Albertini, E. Favaron, M. Zignani, D. Orteschi, P. Bianchi, F. Faravelli, F. Forzano, M. Seri, A. Wischmeijer, D. Turchetti, E. Pompilii, M. Gnoli, G. Cocchi, L. Mazzanti, R. Bergamaschi, D. De Brasi, M.P. Sperandeo, F. Mari, V. Uliana, R. Mostardini, M. Cecconi, M Grasso, S. Sassi, G. Sebastio, A. Renieri, M. Silengo, S. Bernasconi, N. Wakamatsu and G. Neri

    Version of Record online : 12 FEB 2009, DOI: 10.1002/ajmg.a.32693

  8. Epilepsy in Mowat–Wilson syndrome: Delineation of the electroclinical phenotype

    American Journal of Medical Genetics Part A

    Volume 161, Issue 2, February 2013, Pages: 273–284, Duccio Maria Cordelli, Livia Garavelli, Salvatore Savasta, Azzurra Guerra, Alessandro Pellicciari, Lucio Giordano, Silvia Bonetti, Ilaria Cecconi, Anita Wischmeijer, Marco Seri, Simonetta Rosato, Chiara Gelmini, Elvio Della Giustina, Anna Rita Ferrari, Nicoletta Zanotta, Roberta Epifanio, Daniele Grioni, Baris Malbora, Isabella Mammi, Francesca Mari, Sabrina Buoni, Rosa Mostardini, Salvatore Grosso, Chiara Pantaleoni, Morena Doz, Maria Luisa Poch-Olivé, Francesca Rivieri, Giovanni Sorge, Graziella Simonte, Francesca Licata, Luigi Tarani, Emanuela Terazzi, Laura Mazzanti, Paola Cerruti Mainardi, Antonella Boni, Francesca Faravelli, Marina Grasso, Paolo Bianchi, Marcella Zollino and Emilio Franzoni

    Version of Record online : 15 JAN 2013, DOI: 10.1002/ajmg.a.35717

  9. Sleep disturbance in Mowat–Wilson syndrome

    American Journal of Medical Genetics Part A

    Volume 170, Issue 3, March 2016, Pages: 654–660, Elizabeth Evans, David Mowat, Meredith Wilson and Stewart Einfeld

    Version of Record online : 21 DEC 2015, DOI: 10.1002/ajmg.a.37502

  10. You have full text access to this OnlineOpen article
    Experience of Mowat–Wilson syndrome prenatal diagnosis for a Chinese family

    Clinical Case Reports

    Volume 5, Issue 1, January 2017, Pages: 9–13, Qian Jiang, Xiaoxiao Zhang, Yinan Ma, Qi Li, Chunhua Zheng, Yuchun Yan, Zhen Zhang, Ping Xiao, Lin Su, Wei Cheng, Hong Pan and Long Li

    Version of Record online : 17 NOV 2016, DOI: 10.1002/ccr3.741

  11. Polymicrogyria in a 10-month-old boy with Mowat–Wilson syndrome

    American Journal of Medical Genetics Part A

    Volume 167, Issue 10, October 2015, Pages: 2402–2405, Susan B. Murray, Brooke B. Spangler, Benjamin M. Helm and Samantha Schrier Vergano

    Version of Record online : 26 MAY 2015, DOI: 10.1002/ajmg.a.37171

  12. Recurrent structural malformations identified among Mowat–Wilson syndrome fetuses

    Prenatal Diagnosis

    Volume 34, Issue 3, March 2014, Pages: 296–298, Yan Zhou, Jin Huang, Yvonne Kwun Yue Cheng, Tak Yeung Leung, Ritsuko K. Pooh, Fai Man Lo and Kwong Wai Choy

    Version of Record online : 23 DEC 2013, DOI: 10.1002/pd.4292

  13. 35th Annual David W Smith Workshop on Malformations and Morphogenesis: Abstracts of the 2014 Annual Meeting

    American Journal of Medical Genetics Part A

    Volume 167, Issue 8, August 2015, Pages: 1685–1740, Stephen R. Braddock, Robert J. Lipinski, Marc S. Williams and John C. Carey

    Version of Record online : 22 MAY 2015, DOI: 10.1002/ajmg.a.37107

  14. You have full text access to this OnlineOpen article
    Zeb2 Regulates Cell Fate at the Exit from Epiblast State in Mouse Embryonic Stem Cells

    STEM CELLS

    Agata Stryjewska, Ruben Dries, Tim Pieters, Griet Verstappen, Andrea Conidi, Kathleen Coddens, Annick Francis, Lieve Umans, Wilfred F. J. Van IJcken, Geert Berx, Leo A. van Grunsven, Frank G. Grosveld, Steven Goossens, Jody J. Haigh and Danny Huylebroeck

    Version of Record online : 8 NOV 2016, DOI: 10.1002/stem.2521

  15. Autoregulation of ZEB2 expression for zearalenone production in Fusarium graminearum

    Molecular Microbiology

    Volume 97, Issue 5, September 2015, Pages: 942–956, Ae Ran Park, Hokyoung Son, Kyunghun Min, Jinseo Park, Jae Hwan Goo, Sangkee Rhee, Suhn-Kee Chae and Yin-Won Lee

    Version of Record online : 25 JUN 2015, DOI: 10.1111/mmi.13078

  16. Recurrence of Mowat–Wilson syndrome in siblings with a novel mutation in the ZEB2 gene

    American Journal of Medical Genetics Part A

    Volume 146A, Issue 23, 1 December 2008, Pages: 3095–3099, Massimiliano Cecconi, Francesca Forzano, Livia Garavelli, Chiara Pantaleoni, Marina Grasso, Franca Dagna Bricarelli, Lucia Perroni, Emilio Di Maria and Francesca Faravelli

    Version of Record online : 12 NOV 2008, DOI: 10.1002/ajmg.a.32568

  17. Mowat–Wilson syndrome with associated dysphagia

    American Journal of Medical Genetics Part A

    Volume 152A, Issue 2, February 2010, Pages: 484–485, Eloise J. Prijoles and Margaret Adam

    Version of Record online : 25 JAN 2010, DOI: 10.1002/ajmg.a.33211

  18. You have full text access to this Open Access content
    Gene expression profiling of advanced-stage serous ovarian cancers distinguishes novel subclasses and implicates ZEB2 in tumor progression and prognosis

    Cancer Science

    Volume 100, Issue 8, August 2009, Pages: 1421–1428, Kosuke Yoshihara, Atsushi Tajima, Dai Komata, Tadashi Yamamoto, Shoji Kodama, Hiroyuki Fujiwara, Mitsuaki Suzuki, Yoshitaka Onishi, Masayuki Hatae, Kazunobu Sueyoshi, Hisaya Fujiwara, Yoshiki Kudo, Ituro Inoue and Kenichi Tanaka

    Version of Record online : 4 MAY 2009, DOI: 10.1111/j.1349-7006.2009.01204.x

  19. You have free access to this content
    Two different polyketide synthase genes are required for synthesis of zearalenone in Gibberella zeae

    Molecular Microbiology

    Volume 58, Issue 4, November 2005, Pages: 1102–1113, Yong-Tae Kim, Ye-Ryun Lee, Jianming Jin, Kap-Hoon Han, Hun Kim, Jin-Cheol Kim, Theresa Lee, Sung-Hwan Yun and Yin-Won Lee

    Version of Record online : 7 OCT 2005, DOI: 10.1111/j.1365-2958.2005.04884.x

  20. Impact of a Stochastic Kinetic Energy Backscatter scheme across time-scales and resolutions

    Quarterly Journal of the Royal Meteorological Society

    Volume 140, Issue 685, October 2014 Part B, Pages: 2625–2637, Claudio Sanchez, Keith D. Williams, Glenn Shutts and Matthew Collins

    Version of Record online : 9 APR 2014, DOI: 10.1002/qj.2328