rdf:type |
|
lifeskim:mentions |
umls-concept:C0424972,
umls-concept:C0439660,
umls-concept:C0439849,
umls-concept:C0443147,
umls-concept:C0445223,
umls-concept:C1384666,
umls-concept:C1552599,
umls-concept:C1704787,
umls-concept:C1842138,
umls-concept:C2603343,
umls-concept:C2677304
|
pubmed:issue |
6
|
pubmed:dateCreated |
1997-7-10
|
pubmed:abstractText |
To study nonsyndromic progressive sensorineural hearing loss (SNHL) with significant linkage to the DFNA2 locus on chromosome 1p in a Dutch kindred.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
AIM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
0886-4470
|
pubmed:author |
|
pubmed:issnType |
Print
|
pubmed:volume |
123
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
573-7
|
pubmed:dateRevised |
2010-11-18
|
pubmed:meshHeading |
pubmed-meshheading:9193215-Adult,
pubmed-meshheading:9193215-Aged,
pubmed-meshheading:9193215-Audiometry, Pure-Tone,
pubmed-meshheading:9193215-Chromosomes, Human, Pair 1,
pubmed-meshheading:9193215-Female,
pubmed-meshheading:9193215-Genes, Dominant,
pubmed-meshheading:9193215-Genetic Linkage,
pubmed-meshheading:9193215-Hearing Loss, Sensorineural,
pubmed-meshheading:9193215-Humans,
pubmed-meshheading:9193215-Male,
pubmed-meshheading:9193215-Middle Aged,
pubmed-meshheading:9193215-Netherlands,
pubmed-meshheading:9193215-Pedigree,
pubmed-meshheading:9193215-Reflex, Vestibulo-Ocular,
pubmed-meshheading:9193215-Vestibular Function Tests
|
pubmed:year |
1997
|
pubmed:articleTitle |
Inherited nonsyndromic hearing loss. An audiovestibular study in a large family with autosomal dominant progressive hearing loss related to DFNA2.
|
pubmed:affiliation |
Department of Otorhinolaryngology, University Hospital Nijmegen, the Netherlands.
|
pubmed:publicationType |
Journal Article
|