10376574

Source:http://linkedlifedata.com/resource/pubmed/id/10376574

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:C0011053, umls-concept:C0026081, umls-concept:C0026882, umls-concept:C0439660, umls-concept:C0560175, umls-concept:C0678227, umls-concept:C1415077, umls-concept:C1521828, umls-concept:C1706209
pubmed:issue	23
pubmed:dateCreated	1999-6-24
pubmed:abstractText	Mutations in the GJB2 gene are the most common known cause of inherited congenital severe-to-profound deafness. The carrier frequency of these mutations is not known.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/HG-00457, http://linkedlifedata.com/resource/pubmed/grant/R01-DC02842
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7501160
pubmed:citationSubset	AIM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Connexins, http://linkedlifedata.com/resource/pubmed/chemical/connexin 26
pubmed:status	MEDLINE
pubmed:month	Jun
pubmed:issn	0098-7484
pubmed:author	pubmed-author:GreenG EGE, pubmed-author:McDonaldJ MJM, pubmed-author:ScottD ADA, pubmed-author:SheffieldV CVC, pubmed-author:SmithR JRJ, pubmed-author:WoodworthG GGG
pubmed:issnType	Print
pubmed:day	16
pubmed:volume	281
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2211-6
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:10376574-Adolescent, pubmed-meshheading:10376574-Child, pubmed-meshheading:10376574-Child, Preschool, pubmed-meshheading:10376574-Connexins, pubmed-meshheading:10376574-DNA Mutational Analysis, pubmed-meshheading:10376574-Deafness, pubmed-meshheading:10376574-Genes, Recessive, pubmed-meshheading:10376574-Genetic Testing, pubmed-meshheading:10376574-Hearing Loss, Sensorineural, pubmed-meshheading:10376574-Heterozygote, pubmed-meshheading:10376574-Humans, pubmed-meshheading:10376574-Infant, pubmed-meshheading:10376574-Infant, Newborn, pubmed-meshheading:10376574-Midwestern United States, pubmed-meshheading:10376574-Mutation, pubmed-meshheading:10376574-Polymerase Chain Reaction, pubmed-meshheading:10376574-Polymorphism, Single-Stranded Conformational, pubmed-meshheading:10376574-Sensitivity and Specificity, pubmed-meshheading:10376574-Statistics as Topic
pubmed:year	1999
pubmed:articleTitle	Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.
pubmed:affiliation	Department of Otolaryngology, Head and Neck Surgery, University of Iowa Hospitals and Clinics, Iowa City, USA.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S.