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15214010
Source:
http://linkedlifedata.com/resource/pubmed/id/15214010
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60
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0030705
,
umls-concept:C0221025
,
umls-concept:C0332597
,
umls-concept:C0684224
,
umls-concept:C0700287
,
umls-concept:C0796004
,
umls-concept:C1416536
,
umls-concept:C1416689
,
umls-concept:C1689985
,
umls-concept:C2697833
pubmed:issue
2
pubmed:dateCreated
2004-6-23
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Genetic Markers
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
1552-4825
pubmed:author
pubmed-author:FukushimaYoshimitsuY
,
pubmed-author:HaradaNaokiN
,
pubmed-author:KishinoTatsuyaT
,
pubmed-author:KurosawaKenjiK
,
pubmed-author:MatsumotoNaomichiN
,
pubmed-author:MatsumotoTadashiT
,
pubmed-author:MiyakeNorikoN
,
pubmed-author:NagaiToshiroT
,
pubmed-author:NiikawaNorioN
,
pubmed-author:OhashiHirofumiH
,
pubmed-author:OhtaTohruT
,
pubmed-author:ShimokawaOsamuO
,
pubmed-author:ShotelersukVorasukV
,
pubmed-author:YoshiuraKo-IchiroK
pubmed:issnType
Print
pubmed:day
15
pubmed:volume
128A
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
170-2
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:15214010-Abnormalities, Multiple
,
pubmed-meshheading:15214010-Chromosomes, Human, Pair 8
,
pubmed-meshheading:15214010-Facies
,
pubmed-meshheading:15214010-Gene Duplication
,
pubmed-meshheading:15214010-Genetic Markers
,
pubmed-meshheading:15214010-Growth Disorders
,
pubmed-meshheading:15214010-Humans
,
pubmed-meshheading:15214010-In Situ Hybridization, Fluorescence
,
pubmed-meshheading:15214010-Intellectual Disability
,
pubmed-meshheading:15214010-Models, Genetic
,
pubmed-meshheading:15214010-Musculoskeletal Abnormalities
,
pubmed-meshheading:15214010-Phenotype
,
pubmed-meshheading:15214010-Polymorphism, Genetic
,
pubmed-meshheading:15214010-Skin Abnormalities
,
pubmed-meshheading:15214010-Syndrome
pubmed:year
2004
pubmed:articleTitle
On the reported 8p22-p23.1 duplication in Kabuki make-up syndrome (KMS) and its absence in patients with typical KMS.
pubmed:affiliation
Department of Human Genetics, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
pubmed:publicationType
Journal Article