16419134

Source:http://linkedlifedata.com/resource/pubmed/id/16419134

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008928, umls-concept:C0078058, umls-concept:C1256770, umls-concept:C1419771, umls-concept:C1521538, umls-concept:C2675008
pubmed:issue	4
pubmed:dateCreated	2006-1-26
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Core Binding Factor Alpha 1 Subunit, http://linkedlifedata.com/resource/pubmed/chemical/RUNX2 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/VEGFA protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Vascular Endothelial Growth Factor A
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	1552-4825
pubmed:author	pubmed-author:FujiiYasushiY, pubmed-author:HiguchiMasatakaM, pubmed-author:HosokaiNoboruN, pubmed-author:IzumiKosukeK, pubmed-author:KosakiKenjiroK, pubmed-author:KosakiRikaR, pubmed-author:NaitoYokoY, pubmed-author:NishimuraGenG, pubmed-author:TakahashiTakaoT, pubmed-author:YahagiNaohisaN
pubmed:issnType	Print
pubmed:day	15
pubmed:volume	140
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	398-401
pubmed:dateRevised	2007-5-2
pubmed:meshHeading	pubmed-meshheading:16419134-Cardiovascular Abnormalities, pubmed-meshheading:16419134-Chromosomes, Human, Pair 6, pubmed-meshheading:16419134-Cleidocranial Dysplasia, pubmed-meshheading:16419134-Core Binding Factor Alpha 1 Subunit, pubmed-meshheading:16419134-Gene Deletion, pubmed-meshheading:16419134-Humans, pubmed-meshheading:16419134-Infant, pubmed-meshheading:16419134-Male, pubmed-meshheading:16419134-Musculoskeletal Abnormalities, pubmed-meshheading:16419134-Vascular Endothelial Growth Factor A
pubmed:year	2006
pubmed:articleTitle	Cleidocranial dysplasia plus vascular anomalies with 6p21.2 microdeletion spanning RUNX2 and VEGF.
pubmed:publicationType	Letter, Case Reports, Research Support, Non-U.S. Gov't