SEARCH

SEARCH BY CITATION

Cited in:

CrossRef

This article has been cited by:

  1. 1
    Yukiko Arimoto, Kazunori Namba, Atsuko Nakano, Tatsuo Matsunaga, Chronic constipation recognized as a sign of a SOX10 mutation in a patient with Waardenburg syndrome, Gene, 2014, 540, 2, 258

    CrossRef

  2. 2
    Georgios Kontorinis, Friedrich Goetz, Heinrich Lanfermann, Stefan Luytenski, Anja M. Giesemann, Inner ear anatomy in Waardenburg syndrome: Radiological assessment and comparison with normative data, International Journal of Pediatric Otorhinolaryngology, 2014, 78, 8, 1320

    CrossRef

  3. 3
    Stephen J. Broomfield, Iain A. Bruce, Lise Henderson, Richard T. Ramsden, Kevin M.J. Green, Cochlear implantation in children with syndromic deafness, International Journal of Pediatric Otorhinolaryngology, 2013, 77, 8, 1312

    CrossRef

  4. 4
    John Greinwald, Alessandro deAlarcon, Aliza Cohen, Trina Uwiera, Keijan Zhang, Corning Benton, Mark Halstead, Jareen Meinzen-Derr, Significance of unilateral enlarged vestibular aqueduct, The Laryngoscope, 2013, 123, 6
  5. 5
    M. Elmaleh-Berges, C. Baumann, N. Noel-Petroff, A. Sekkal, V. Couloigner, K. Devriendt, M. Wilson, S. Marlin, G. Sebag, V. Pingault, Spectrum of Temporal Bone Abnormalities in Patients with Waardenburg Syndrome and SOX10 Mutations, American Journal of Neuroradiology, 2013, 34, 6, 1257

    CrossRef

  6. 6
    Rena Ellen Falk, Arti Pandya, Emery and Rimoin's Principles and Practice of Medical Genetics, 2013,

    CrossRef

  7. 7
    B. Y. Huang, C. Zdanski, M. Castillo, Pediatric Sensorineural Hearing Loss, Part 2: Syndromic and Acquired Causes, American Journal of Neuroradiology, 2012, 33, 3, 399

    CrossRef

  8. 8
    Taku Ito, Byung Yoon Choi, Kelly A. King, Christopher K. Zalewski, Julie Muskett, Parna Chattaraj, Thomas Shawker, James C. Reynolds, John A. Butman, Carmen C. Brewer, Philine Wangemann, Seth L. Alper, Andrew J. Griffith, <i>SLC26A4</i> Genotypes and Phenotypes Associated with Enlargement of the Vestibular Aqueduct, Cellular Physiology and Biochemistry, 2011, 28, 3, 545

    CrossRef

  9. 9
    Georgios Kontorinis, Thomas Lenarz, Alexandros Giourgas, Martin Durisin, Anke Lesinski-Schiedat, Outcomes and Special Considerations of Cochlear Implantation in Waardenburg Syndrome, Otology & Neurotology, 2011, 32, 6, 951

    CrossRef

  10. 10
    Véronique Pingault, Dorothée Ente, Florence Dastot-Le Moal, Michel Goossens, Sandrine Marlin, Nadège Bondurand, Review and update of mutations causing Waardenburg syndrome, Human Mutation, 2010, 31, 4
  11. 11
    L.A. Schimmenti, Christina G.S. Palmer, Molecular Diagnostics, 2010,

    CrossRef

  12. 12
    Kenneth H. Lee, Daniel A. Larson, Gordon Shott, Brian Rasmussen, Aliza P. Cohen, Corning Benton, Mark Halsted, Daniel Choo, Jareen Meinzen-Derr, John H. Greinwald, Audiologic and temporal bone imaging findings in patients with sensorineural hearing loss and GJB2 mutations, The Laryngoscope, 2009, 119, 3
  13. 13
    Ingrid Breuskin, Morgan Bodson, Nicolas Thelen, Marc Thiry, Laurence Borgs, Laurent Nguyen, Philippe P. Lefebvre, Brigitte Malgrange, Sox10 promotes the survival of cochlear progenitors during the establishment of the organ of Corti, Developmental Biology, 2009, 335, 2, 327

    CrossRef

  14. 14
    Virendra N. Sehgal, Govind Srivastava, Hereditary hypo/de-pigmented dermatoses: An overview, International Journal of Dermatology, 2008, 0, 0, 080521053359321

    CrossRef

  15. 15
    Virendra N. Sehgal, Govind Srivastava, Hereditary hypo/de-pigmented dermatoses: An overview, International Journal of Dermatology, 2008, 47, 10
  16. 16
    Oana Vele, Iris Schrijver, Inherited hearing loss: molecular genetics and diagnostic testing, Expert Opinion on Medical Diagnostics, 2008, 2, 3, 231

    CrossRef

  17. 17
    Robert D. Cullen, Carlton Zdanski, Patricia Roush, Carolyn Brown, Holly Teagle, Harold C. Pillsbury, Craig Buchman, Cochlear Implants in Waardenburg Syndrome, The Laryngoscope, 2006, 116, 7
  18. 18
    Caroline D. Robson, Congenital hearing impairment, Pediatric Radiology, 2006, 36, 4, 309

    CrossRef

  19. 19
    José Ángel González-García, Andrés Ibáñez, Rafael Ramírez-Camacho, Antonio Rodríguez, José Ramón García-Berrocal, Almudena Trinidad, Enlarged vestibular aqueduct: looking for genotypic–phenotypic correlations, European Archives of Oto-Rhino-Laryngology, 2006, 263, 11, 971

    CrossRef

  20. 20
    Taku Ito, Yoshihiro Noguchi, Takatoshi Yashima, Ken Kitamura, SIX1 Mutation Associated With Enlargement of the Vestibular Aqueduct in a Patient With Branchio-Oto Syndrome, The Laryngoscope, 2006, 116, 5
  21. 21
    Silke Steinbach, Steffi-Johanna Brockmeier, >Jan Kiefer, The large vestibular aqueduct – case report and review of the literature, Acta Oto-laryngologica, 2006, 126, 8, 788

    CrossRef

  22. 22
    N Loundon, I Rouillon, N Munier, S Marlin, G Roger, E N Garabedian, Cochlear Implantation in Children with Internal Ear Malformations, Otology & Neurotology, 2005, 26, 4, 668

    CrossRef

  23. 23
    Simon Edelstein, Thomas P Naidich, T.Hans Newton, The rare phakomatoses, Neuroimaging Clinics of North America, 2004, 14, 2, 185

    CrossRef