14757865

Source:http://linkedlifedata.com/resource/pubmed/id/14757865

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015576, umls-concept:C0026882, umls-concept:C0265259, umls-concept:C0557775, umls-concept:C1416474, umls-concept:C1511780, umls-concept:C2919108
pubmed:issue	2
pubmed:dateCreated	2004-2-3
pubmed:databankReference	http://linkedlifedata.com/resource/pubmed/xref/OMIM/119300, http://linkedlifedata.com/resource/pubmed/xref/OMIM/119500
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985087R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA, http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/IRF6 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Interferon Regulatory Factors, http://linkedlifedata.com/resource/pubmed/chemical/Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	1468-6244
pubmed:author	pubmed-author:BayenHH, pubmed-author:GhassibéMM, pubmed-author:GillerotYY, pubmed-author:RevencuNN, pubmed-author:VanwijckRR, pubmed-author:Verellen-DumoulinCC, pubmed-author:VikkulaMM
pubmed:issnType	Electronic
pubmed:volume	41
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	e15
pubmed:dateRevised	2010-11-18
pubmed:meshHeading	pubmed-meshheading:14757865-Abnormalities, Multiple, pubmed-meshheading:14757865-Anodontia, pubmed-meshheading:14757865-Chromosomes, Human, Pair 1, pubmed-meshheading:14757865-Cleft Lip, pubmed-meshheading:14757865-Cleft Palate, pubmed-meshheading:14757865-DNA, pubmed-meshheading:14757865-DNA-Binding Proteins, pubmed-meshheading:14757865-Female, pubmed-meshheading:14757865-Foot Deformities, Congenital, pubmed-meshheading:14757865-Genes, Dominant, pubmed-meshheading:14757865-Genetic Linkage, pubmed-meshheading:14757865-Humans, pubmed-meshheading:14757865-Interferon Regulatory Factors, pubmed-meshheading:14757865-Lip, pubmed-meshheading:14757865-Male, pubmed-meshheading:14757865-Mutation, pubmed-meshheading:14757865-Pedigree, pubmed-meshheading:14757865-Protein Binding, pubmed-meshheading:14757865-Protein Structure, Tertiary, pubmed-meshheading:14757865-Proteins, pubmed-meshheading:14757865-Syndrome, pubmed-meshheading:14757865-Transcription Factors, pubmed-meshheading:14757865-Uvula
pubmed:year	2004
pubmed:articleTitle	Six families with van der Woude and/or popliteal pterygium syndrome: all with a mutation in the IRF6 gene.
pubmed:affiliation	Laboratory of Human Molecular Genetics, Christian de Duve Institute of Cellular Pathology and Universite catholique de Louvain, Avenue Hippocrate 74+4, Brussels, Belgium.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't