17256794

Source:http://linkedlifedata.com/resource/pubmed/id/17256794

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0019904, umls-concept:C0026882, umls-concept:C0337493, umls-concept:C0678227, umls-concept:C1384666, umls-concept:C1415077, umls-concept:C2931198
pubmed:issue	4
pubmed:dateCreated	2007-2-1
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/DC 005575
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Connexins, http://linkedlifedata.com/resource/pubmed/chemical/connexin 26
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	1552-4825
pubmed:author	pubmed-author:AngeliSimon ISI, pubmed-author:DuLi LinLL, pubmed-author:LiuXue ZongXZ, pubmed-author:OuyangXiao MeiXM, pubmed-author:YanDeniseD
pubmed:issnType	Print
pubmed:day	15
pubmed:volume	143
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	385-6
pubmed:dateRevised	2007-12-3
pubmed:meshHeading	pubmed-meshheading:17256794-Chromosomes, Human, Pair 13, pubmed-meshheading:17256794-Connexins, pubmed-meshheading:17256794-Female, pubmed-meshheading:17256794-Gene Frequency, pubmed-meshheading:17256794-Hearing Loss, pubmed-meshheading:17256794-Homozygote, pubmed-meshheading:17256794-Humans, pubmed-meshheading:17256794-Male, pubmed-meshheading:17256794-Sequence Deletion, pubmed-meshheading:17256794-Uniparental Disomy
pubmed:year	2007
pubmed:articleTitle	Paternal uniparental disomy of chromosome 13 causing homozygous 35delG mutation of the GJB2 gene and hearing loss.
pubmed:affiliation	Department of Otolaryngology, University of Miami, Miami, Florida 33136, USA.
pubmed:publicationType	Journal Article, Research Support, N.I.H., Extramural