Temporal bone abnormalities in children with GJB2 mutations

Laryngoscope

Volumn 121, Issue 3, 2011, Pages 630-635

  Kenna, Margaret A ^a,b   Rehm, Heidi L ^a,b,c   Frangulov, Anna ^a   Feldman, Henry A ^a   Robson, Caroline D ^a  

^a BOSTON CHILDREN S HOSPITAL   (United States)

^b HARVARD MEDICAL SCHOOL   (United States)

^c LABORATORY FOR MOLECULAR MEDICINE   (United States)

Author keywords

Computed tomography; Connexin 26; GJB2; magnetic resonance imaging; sensorineural hearing loss; temporal bones

Indexed keywords

CONNEXIN 26;

ARTICLE; BONE MALFORMATION; CHILDHOOD DISEASE; COCHLEAR NERVE; COHORT ANALYSIS; COMPUTER ASSISTED TOMOGRAPHY; CONTROLLED STUDY; CORRELATION ANALYSIS; DISEASE SEVERITY; GENOTYPE; HEALTH DISPARITY; HUMAN; HUMAN CELL; INFANT; INTERNAL AUDITORY CANAL; MAJOR CLINICAL STUDY; MORBIDITY; MUTATION; NUCLEAR MAGNETIC RESONANCE IMAGING; OBSERVATIONAL STUDY; PATHOGENESIS; PERCEPTION DEAFNESS; PRIORITY JOURNAL; RETROSPECTIVE STUDY; SEMICIRCULAR CANAL; TEMPORAL BONE;

ADOLESCENT; ALLELES; CHILD; CHILD, PRESCHOOL; COCHLEA; COCHLEAR NERVE; COHORT STUDIES; CONNEXINS; DEAFNESS; DNA MUTATIONAL ANALYSIS; FEMALE; GENOTYPE; HEARING LOSS, MIXED CONDUCTIVE-SENSORINEURAL; HEARING LOSS, SENSORINEURAL; HUMANS; INFANT; MAGNETIC RESONANCE IMAGING; MALE; PETROUS BONE; SEMICIRCULAR CANALS; STATISTICS AS TOPIC; TEMPORAL BONE; TOMOGRAPHY, X-RAY COMPUTED; YOUNG ADULT;

EID: 79951926435     PISSN: 0023852X     EISSN: None     Source Type: Journal    
DOI: 10.1002/lary.21414     Document Type: Article

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