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16283890
Source:
http://linkedlifedata.com/resource/pubmed/id/16283890
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0020792
,
umls-concept:C0024796
,
umls-concept:C0026882
,
umls-concept:C0030705
,
umls-concept:C0205314
,
umls-concept:C0439658
,
umls-concept:C0439858
,
umls-concept:C0596611
,
umls-concept:C0679622
,
umls-concept:C0919538
,
umls-concept:C1556095
,
umls-concept:C1836635
pubmed:issue
6
pubmed:dateCreated
2005-11-14
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/16283890-15235604
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/0253664
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/Microfilament Proteins
,
http://linkedlifedata.com/resource/pubmed/chemical/Protein-Serine-Threonine Kinases
,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Transforming Growth...
,
http://linkedlifedata.com/resource/pubmed/chemical/fibrillin
,
http://linkedlifedata.com/resource/pubmed/chemical/transforming growth factor-beta...
pubmed:status
MEDLINE
pubmed:month
Dec
pubmed:issn
0009-9163
pubmed:author
pubmed-author:ChaKK
,
pubmed-author:ChangS HSH
,
pubmed-author:ChoiJ-HJH
,
pubmed-author:HorS SSS
,
pubmed-author:KimJ-EJE
,
pubmed-author:KimJ-WJW
,
pubmed-author:MOCKH EHE
,
pubmed-author:ParkI SIS
,
pubmed-author:YooH-WHW
pubmed:issnType
Print
pubmed:volume
68
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
561-3
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:16283890-Abnormalities, Multiple
,
pubmed-meshheading:16283890-Amino Acid Sequence
,
pubmed-meshheading:16283890-Aortic Aneurysm
,
pubmed-meshheading:16283890-Base Sequence
,
pubmed-meshheading:16283890-Coronary Angiography
,
pubmed-meshheading:16283890-DNA Mutational Analysis
,
pubmed-meshheading:16283890-Gene Frequency
,
pubmed-meshheading:16283890-Genetic Testing
,
pubmed-meshheading:16283890-Haplotypes
,
pubmed-meshheading:16283890-Humans
,
pubmed-meshheading:16283890-Korea
,
pubmed-meshheading:16283890-Marfan Syndrome
,
pubmed-meshheading:16283890-Microfilament Proteins
,
pubmed-meshheading:16283890-Mutation
,
pubmed-meshheading:16283890-Pedigree
,
pubmed-meshheading:16283890-Protein-Serine-Threonine Kinases
,
pubmed-meshheading:16283890-Receptors, Transforming Growth Factor beta
,
pubmed-meshheading:16283890-Syndrome
pubmed:year
2005
pubmed:articleTitle
Identification of a novel TGFBR2 gene mutation in a Korean patient with Loeys-Dietz aortic aneurysm syndrome; no mutation in TGFBR2 gene in 30 patients with classic Marfan's syndrome.
pubmed:publicationType
Letter
,
Comment
,
Case Reports
,
Research Support, Non-U.S. Gov't