Research ArticlePediatrics
Spectrum of Temporal Bone Abnormalities in Patients with Waardenburg Syndrome and SOX10 Mutations
M. Elmaleh-Bergès, C. Baumann, N. Noël-Pétroff, A. Sekkal, V. Couloigner, K. Devriendt, M. Wilson, S. Marlin, G. Sebag and V. Pingault
American Journal of Neuroradiology June 2013, 34 (6) 1257-1263; DOI: https://doi.org/10.3174/ajnr.A3367
M. Elmaleh-Bergès
aFrom the Departments of Pediatric Imaging (M.E.-B., A.S., G.S.)
C. Baumann
bClinical Genetics (C.B.)
N. Noël-Pétroff
cOtorhinolaryngology (N.N.-P.), Hôpital Robert Debré, Paris, France
A. Sekkal
aFrom the Departments of Pediatric Imaging (M.E.-B., A.S., G.S.)
V. Couloigner
eDepartment of Otorhinolaryngology (V.C.), Hôpital Necker-Enfants Malades, Paris, France
K. Devriendt
dCenter for Human Genetics (K.D.), University Hospitals Leuven, Leuven, Belgium
M. Wilson
fDepartment of Clinical Genetics (M.W.), The Children's Hospital at Westmead, Sydney, Australia
S. Marlin
gCentre de Référence des Surdités Génétiques (S.M.), Hôpital Armand-Trousseau, Paris, France
G. Sebag
aFrom the Departments of Pediatric Imaging (M.E.-B., A.S., G.S.)
V. Pingault
hLaboratoire de Biochimie et Génétique (V.P.), AP-HP, Hôpital Henri Mondor–Albert Chenevier, Créteil, France.
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