rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
8
|
pubmed:dateCreated |
2003-8-19
|
pubmed:abstractText |
To determine the genotypic and phenotypic correlations of hearing impairment (HI) in a midwestern US population related to autosomal recessive nonsyndromic hearing loss locus 1 (DFNB1).
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pubmed:language |
eng
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pubmed:journal |
|
pubmed:citationSubset |
AIM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
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pubmed:month |
Aug
|
pubmed:issn |
0886-4470
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pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
129
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
836-40
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:12925341-Adolescent,
pubmed-meshheading:12925341-Audiometry, Pure-Tone,
pubmed-meshheading:12925341-Chi-Square Distribution,
pubmed-meshheading:12925341-Child,
pubmed-meshheading:12925341-Connexins,
pubmed-meshheading:12925341-Female,
pubmed-meshheading:12925341-Gene Frequency,
pubmed-meshheading:12925341-Genes, Recessive,
pubmed-meshheading:12925341-Genotype,
pubmed-meshheading:12925341-Hearing Loss, Sensorineural,
pubmed-meshheading:12925341-Humans,
pubmed-meshheading:12925341-Male,
pubmed-meshheading:12925341-Midwestern United States,
pubmed-meshheading:12925341-Mutation,
pubmed-meshheading:12925341-Phenotype,
pubmed-meshheading:12925341-Prevalence,
pubmed-meshheading:12925341-Retrospective Studies
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pubmed:year |
2003
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pubmed:articleTitle |
Genotypic and phenotypic correlations of DFNB1-related hearing impairment in the Midwestern United States.
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pubmed:affiliation |
Center for Hearing and Deafness Research, Cincinnati, Ohio, USA.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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