11883438

Source:http://linkedlifedata.com/resource/pubmed/id/11883438

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0026882, umls-concept:C0039082, umls-concept:C0041432, umls-concept:C0042593, umls-concept:C0271829, umls-concept:C0302559
pubmed:issue	1
pubmed:dateCreated	2002-3-7
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7610513
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Carrier Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Membrane Transport Proteins, http://linkedlifedata.com/resource/pubmed/chemical/SLC26A4 protein, human
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	0381-6605
pubmed:author	pubmed-author:CucciRobert ARA, pubmed-author:MacNeillChristineC, pubmed-author:ParnesLorne SLS, pubmed-author:SmithRichard J HRJ, pubmed-author:VescanAllanA
pubmed:issnType	Print
pubmed:volume	31
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	54-7
pubmed:dateRevised	2004-11-17
pubmed:meshHeading	pubmed-meshheading:11883438-Carrier Proteins, pubmed-meshheading:11883438-Child, Preschool, pubmed-meshheading:11883438-Cochlear Implantation, pubmed-meshheading:11883438-Deafness, pubmed-meshheading:11883438-Humans, pubmed-meshheading:11883438-Male, pubmed-meshheading:11883438-Membrane Transport Proteins, pubmed-meshheading:11883438-Mutation, pubmed-meshheading:11883438-Syndrome, pubmed-meshheading:11883438-Twins, Monozygotic, pubmed-meshheading:11883438-Vestibular Aqueduct, pubmed-meshheading:11883438-Vestibular Diseases
pubmed:year	2002
pubmed:articleTitle	Cochlear implantation and Pendred's syndrome mutation in monozygotic twins with large vestibular aqueduct syndrome.
pubmed:affiliation	Department of Otolaryngology, University of Western Ontario, London Health Sciences Centre.
pubmed:publicationType	Journal Article, Case Reports