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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
9
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pubmed:dateCreated |
2011-8-12
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pubmed:abstractText |
To determine the clinical sensitivity of DFNB1 genetic testing (analysis of the connexin 26 gene GJB2) for non-syndromic sensorineural hearing loss (SNHL) in British Pakistani children and extend to a comparison with British White children and literature data.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
AIM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Sep
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pubmed:issn |
1468-2044
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pubmed:author |
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pubmed:issnType |
Electronic
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pubmed:volume |
96
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
798-803
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pubmed:meshHeading |
pubmed-meshheading:21586435-Adolescent,
pubmed-meshheading:21586435-Asian Continental Ancestry Group,
pubmed-meshheading:21586435-Child,
pubmed-meshheading:21586435-Child, Preschool,
pubmed-meshheading:21586435-Connexins,
pubmed-meshheading:21586435-England,
pubmed-meshheading:21586435-European Continental Ancestry Group,
pubmed-meshheading:21586435-Female,
pubmed-meshheading:21586435-Genetic Predisposition to Disease,
pubmed-meshheading:21586435-Hearing Loss, Sensorineural,
pubmed-meshheading:21586435-Humans,
pubmed-meshheading:21586435-Infant,
pubmed-meshheading:21586435-Infant, Newborn,
pubmed-meshheading:21586435-Male,
pubmed-meshheading:21586435-Mutation,
pubmed-meshheading:21586435-Retrospective Studies
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pubmed:year |
2011
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pubmed:articleTitle |
Low prevalence of DFNB1 (connexin 26) mutations in British Pakistani children with non-syndromic sensorineural hearing loss.
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pubmed:affiliation |
St Luke's Hospital, Little Horton Lane, Bradford BD5 0NA, UK. soo.yoong@bradfordhospitals.nhs.uk
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pubmed:publicationType |
Journal Article
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