Research ArticlePediatric Neuroimaging
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.

Submit a Response to This Article
Jump to comment:
No eLetters have been published for this article.
In this issue
Advertisement
M. Elmaleh-Bergès, C. Baumann, N. Noël-Pétroff, 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 Jun 2013, 34 (6) 1257-1263; DOI: 10.3174/ajnr.A3367
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, V. Pingault
American Journal of Neuroradiology Jun 2013, 34 (6) 1257-1263; DOI: 10.3174/ajnr.A3367
Jump to section
Related Articles
Cited By...
- The RNA-binding protein TRIM71 is essential for hearing in humans and mice and regulates the timing of auditory sensory organ development
- SOX10: 20 years of phenotypic plurality and current understanding of its developmental function
- GENETICS IN ENDOCRINOLOGY: Genetic counseling for congenital hypogonadotropic hypogonadism and Kallmann syndrome: new challenges in the era of oligogenism and next-generation sequencing
- Olfactory bulb agenesis with normal sexual hormones
- Spectrum of Clinical and Associated MR Imaging Findings in Children with Olfactory Anomalies
This article has not yet been cited by articles in journals that are participating in Crossref Cited-by Linking.
More in this TOC Section
Similar Articles
Advertisement