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British Journal of Radiology, ISSN 0007-1285, 09/2011, Volume 84, Issue 1005, pp. 859 - 863
Journal Article
American Journal of Neuroradiology, ISSN 0195-6108, 06/2013, Volume 34, Issue 6, pp. 1257 - 1263
BACKGROUND AND PURPOSE: Waardenburg syndrome, characterized by deafness and pigmentation abnormalities, is clinically and genetically heterogeneous, consisting... 
INNER-EAR | TYPE-4 | SENSORINEURAL HEARING-LOSS | GENE | HISTOPATHOLOGIC FINDINGS | HIRSCHSPRUNG-DISEASE | EXPRESSION | ASSOCIATION | NEUROIMAGING | RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING | TRUNCATING MUTATIONS | CLINICAL NEUROLOGY | Olfactory Bulb - diagnostic imaging | Cochlea - diagnostic imaging | Semicircular Canals - pathology | Waardenburg Syndrome - diagnostic imaging | Humans | Temporal Bone - abnormalities | Child, Preschool | Semicircular Canals - abnormalities | Infant | Male | Ear, Inner - pathology | Young Adult | Parotid Gland - abnormalities | Cochlear Nerve - pathology | Adult | Female | Retrospective Studies | Child | Infant, Newborn | Diagnosis, Differential | Temporal Bone - diagnostic imaging | Olfactory Bulb - pathology | Parotid Gland - diagnostic imaging | Ear, Inner - diagnostic imaging | Hearing Loss, Sensorineural - pathology | Waardenburg Syndrome - pathology | Cochlear Nerve - abnormalities | Hearing Loss, Sensorineural - genetics | Hearing Loss, Sensorineural - diagnostic imaging | Parotid Gland - pathology | Radiography | Temporal Bone - pathology | Cochlear Nerve - diagnostic imaging | Waardenburg Syndrome - genetics | Cochlea - pathology | Adolescent | Ear, Inner - abnormalities | Semicircular Canals - diagnostic imaging | Cochlea - abnormalities | Mutation | Olfactory Bulb - abnormalities | SOXE Transcription Factors - genetics
Journal Article
Pediatric Nephrology, ISSN 0931-041X, 2009, Volume 24, Issue 11, pp. 2147 - 2153
Journal Article
Nature, ISSN 0028-0836, 04/2005, Volume 434, Issue 7036, pp. 1031 - 1035
Journal Article
Journal Article
Otology and Neurotology, ISSN 1531-7129, 2016, Volume 37, Issue 9, pp. 1370 - 1375
Objective:To determine the pediatric incidence and association of superior semicircular canal dehiscence (SSCD) with inner ear (IE) anomalies.Study... 
Pediatric superior semicircular canal dehiscence | Inner ear anomalies | Congenital inner ear malformation | SSCD | TEMPORAL BONE | OTORHINOLARYNGOLOGY | PREVALENCE | CLINICAL NEUROLOGY | CHILDREN | Humans | Ear, Inner - abnormalities | Male | Tomography, X-Ray Computed | Retrospective Studies | Child | Labyrinth Diseases - epidemiology | Incidence
Journal Article
British Journal of Radiology, ISSN 0007-1285, 01/2011, Volume 84, Issue 1005, pp. 859 - 863
The aetiology of profound hearing loss in children is complex and multifactorial. Congenital inner ear abnormality is a major cause of hearing loss in... 
Embryology | Reviews | Temporal bone | Computed tomography | Children | Bone imaging | Inner ear | Hearing loss
Journal Article