|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
3
|
|
pubmed:dateCreated |
2006-1-30
|
|
pubmed:abstractText |
Children with severe to profound sensorineural hearing loss due to GJB2 mutations have often been deemed good cochlear implant candidates. Studies on children with GJB2 mutations and cochlear implants have typically excluded children with additional disabilities.
|
|
pubmed:grant |
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Mar
|
|
pubmed:issn |
0165-5876
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
70
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
493-500
|
|
pubmed:dateRevised |
2008-9-3
|
|
pubmed:meshHeading |
pubmed-meshheading:16154643-Adolescent,
pubmed-meshheading:16154643-Apraxias,
pubmed-meshheading:16154643-Attention Deficit Disorder with Hyperactivity,
pubmed-meshheading:16154643-Child,
pubmed-meshheading:16154643-Child, Preschool,
pubmed-meshheading:16154643-Cochlear Implantation,
pubmed-meshheading:16154643-Connexins,
pubmed-meshheading:16154643-Female,
pubmed-meshheading:16154643-Gene Deletion,
pubmed-meshheading:16154643-Hearing Loss, Sensorineural,
pubmed-meshheading:16154643-Humans,
pubmed-meshheading:16154643-Infant,
pubmed-meshheading:16154643-Language Development Disorders,
pubmed-meshheading:16154643-Male,
pubmed-meshheading:16154643-Mutism,
pubmed-meshheading:16154643-Point Mutation
|
|
pubmed:year |
2006
|
|
pubmed:articleTitle |
GJB2 mutations and additional disabilities in a pediatric cochlear implant population.
|
|
pubmed:affiliation |
Division of Developmental Disabilities, Cincinnati Children's Hospital Medical Center, University of Cincinnati, OH 45229, USA. susan.wiley@cchmc.org
|
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
|
