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Research ArticlePediatric Neuroimaging

Abnormal Basiocciput Development in CHARGE Syndrome

K. Fujita, N. Aida, Y. Asakura, K. Kurosawa, T. Niwa, K. Muroya, M. Adachi, G. Nishimura and T. Inoue
American Journal of Neuroradiology March 2009, 30 (3) 629-634; DOI: https://doi.org/10.3174/ajnr.A1380
K. Fujita
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N. Aida
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Y. Asakura
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K. Kurosawa
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T. Niwa
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K. Muroya
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M. Adachi
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G. Nishimura
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T. Inoue
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American Journal of Neuroradiology: 30 (3)
American Journal of Neuroradiology
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Cite this article
K. Fujita, N. Aida, Y. Asakura, K. Kurosawa, T. Niwa, K. Muroya, M. Adachi, G. Nishimura, T. Inoue
Abnormal Basiocciput Development in CHARGE Syndrome
American Journal of Neuroradiology Mar 2009, 30 (3) 629-634; DOI: 10.3174/ajnr.A1380

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Abnormal Basiocciput Development in CHARGE Syndrome
K. Fujita, N. Aida, Y. Asakura, K. Kurosawa, T. Niwa, K. Muroya, M. Adachi, G. Nishimura, T. Inoue
American Journal of Neuroradiology Mar 2009, 30 (3) 629-634; DOI: 10.3174/ajnr.A1380
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  • Coronal Clival Cleft in CHARGE Syndrome: Fetal MRI Series
  • Cerebellar Heterotopias: Expanding the Phenotype of Cerebellar Dysgenesis in CHARGE Syndrome
  • Imaging of Clival Hypoplasia in CHARGE Syndrome and Hypothesis for Development: A Case-Control Study
  • Clival Malformations in CHARGE Syndrome
  • Head and Neck MRI Findings in CHARGE Syndrome
  • Spectrum of Clinical and Associated MR Imaging Findings in Children with Olfactory Anomalies
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  • Mutation update on the CHD7 gene involved in CHARGE syndrome
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    Human Mutation 2012 33 8
  • A novel classification system to predict the pathogenic effects of CHD7 missense variants in CHARGE syndrome
    Jorieke E.H. Bergman, Nicole Janssen, Almer M. van der Sloot, Hermien E.K. de Walle, Jeroen Schoots, Nanna D. Rendtorff, Lisbeth Tranebjaerg, Lies H. Hoefsloot, Conny M.A. van Ravenswaaij-Arts, Robert M.W. Hofstra
    Human Mutation 2012 33 8
  • Chromodomain proteins in development: lessons from CHARGE syndrome
    WS Layman, EA Hurd, DM Martin
    Clinical Genetics 2010 78 1
  • Chiari Malformation Type I: A Case-Control Association Study of 58 Developmental Genes
    Aintzane Urbizu, Claudio Toma, Maria A. Poca, Juan Sahuquillo, Ester Cuenca-León, Bru Cormand, Alfons Macaya, Joerg-Christian Tonn
    PLoS ONE 2013 8 2
  • Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss
    G. Bademci, F. B. Cengiz, J. Foster II, D. Duman, L. Sennaroglu, O. Diaz-Horta, T. Atik, T. Kirazli, L. Olgun, H. Alper, I. Menendez, I. Loclar, G. Sennaroglu, S. Tokgoz-Yilmaz, S. Guo, Y. Olgun, N. Mahdieh, M. Bonyadi, N. Bozan, A. Ayral, F. Ozkinay, M. Yildirim-Baylan, S. H. Blanton, M. Tekin
    Scientific Reports 2016 6 1
  • Mutations in the CHD7 Gene: The Experience of a Commercial Laboratory
    Cynthia F. Bartels, Cheryl Scacheri, Lashonda White, Peter C. Scacheri, Sherri Bale
    Genetic Testing and Molecular Biomarkers 2010 14 6
  • The chromatin remodeling protein CHD7, mutated in CHARGE syndrome, is necessary for proper craniofacial and tracheal development
    Ethan D. Sperry, Elizabeth A. Hurd, Mark A. Durham, Elyse N. Reamer, Adam B. Stein, Donna M. Martin
    Developmental Dynamics 2014 243 9
  • Head and Neck MRI Findings in CHARGE Syndrome
    M.J. Hoch, S.H. Patel, D. Jethanamest, W. Win, G.M. Fatterpekar, J.T. Roland, M. Hagiwara
    American Journal of Neuroradiology 2017 38 12
  • Guidelines in CHARGE syndrome and the missing link: Cranial imaging
    Christa M. de Geus, Rolien H. Free, Berit M. Verbist, Deborah A. Sival, Kim D. Blake, Linda C. Meiners, Conny M. A. van Ravenswaaij‐Arts
    American Journal of Medical Genetics Part C: Seminars in Medical Genetics 2017 175 4
  • Venous malformations of the temporal bone are a common feature in CHARGE syndrome
    David R. Friedmann, Misha Amoils, John A. Germiller, Lawrence R. Lustig, Christine M. Glastonbury, Bidyut K. Pramanik, Anil K. Lalwani
    The Laryngoscope 2012 122 4

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