18553519

Source:http://linkedlifedata.com/resource/pubmed/id/18553519

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017337, umls-concept:C0026882, umls-concept:C0030705, umls-concept:C0796004, umls-concept:C1704259, umls-concept:C1705987
pubmed:issue	14
pubmed:dateCreated	2008-6-23
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	1552-4833
pubmed:author	pubmed-author:FukushimaYoshimitsuY, pubmed-author:KondohTasturoT, pubmed-author:KunibaHideoH, pubmed-author:KurosawaKenjiK, pubmed-author:MatsumotoNaomichiN, pubmed-author:MatsumotoTadashiT, pubmed-author:MiyakeNorikoN, pubmed-author:NagaiToshiroT, pubmed-author:NaritomiKenjiK, pubmed-author:NiikawaNorioN, pubmed-author:OhashiHirofumiH, pubmed-author:OkamotoNobuhikoN, pubmed-author:SatoDaisukeD, pubmed-author:YoshiuraKoh-ichiroK
pubmed:issnType	Electronic
pubmed:day	15
pubmed:volume	146A
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1893-6
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:18553519-Abnormalities, Multiple, pubmed-meshheading:18553519-Amino Acid Substitution, pubmed-meshheading:18553519-Craniofacial Abnormalities, pubmed-meshheading:18553519-DNA Mutational Analysis, pubmed-meshheading:18553519-Female, pubmed-meshheading:18553519-Genes, ras, pubmed-meshheading:18553519-Humans, pubmed-meshheading:18553519-Intellectual Disability, pubmed-meshheading:18553519-MAP Kinase Signaling System, pubmed-meshheading:18553519-Male, pubmed-meshheading:18553519-Mutation, pubmed-meshheading:18553519-Point Mutation, pubmed-meshheading:18553519-Syndrome
pubmed:year	2008
pubmed:articleTitle	No mutation in RAS-MAPK pathway genes in 30 patients with Kabuki syndrome.
pubmed:affiliation	Department of Human Genetics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't