GJB2 mutations and additional disabilities in a pediatric cochlear implant population

International Journal of Pediatric Otorhinolaryngology

Volumn 70, Issue 3, 2006, Pages 493-500

  Wiley, S ^a   Choo, D ^b   Meinzen Derr, J ^c   Hilbert, L ^c   Greinwald, J ^b  

^a UNIVERSITY OF CINCINNATI   (United States)

^b UNIVERSITY OF CINCINNATI COLLEGE OF MEDICINE   (United States)

^c CINCINNATI CHILDREN'S HOSPITAL MEDICAL CENTER   (United States)

Author keywords

Connexin 26; GJB2; Multi handicap; Pediatric cochlear implantation; Sensorineural hearing loss

Indexed keywords

ALLELE; APHASIA; APRAXIA; ATTENTION DEFICIT DISORDER; AUTISM; CHILD; COCHLEA PROSTHESIS; CONTROLLED STUDY; DEVELOPMENTAL DISORDER; FEMALE; GENE; GENE MUTATION; GENOTYPE; GJB2 GENE; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; LANGUAGE DISABILITY; LEARNING DISORDER; MAJOR CLINICAL STUDY; MALE; MOTOR DYSFUNCTION; PERCEPTION DEAFNESS; PREOPERATIVE EVALUATION; PRIORITY JOURNAL; RETROSPECTIVE STUDY; REVIEW; RISK FACTOR;

EID: 31544444961     PISSN: 01655876     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijporl.2005.07.026     Document Type: Article

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