20949626

Source:http://linkedlifedata.com/resource/pubmed/id/20949626

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0017337, umls-concept:C0023798, umls-concept:C0030705, umls-concept:C0039685, umls-concept:C0040715, umls-concept:C0332256, umls-concept:C0558295, umls-concept:C0599718, umls-concept:C0599813, umls-concept:C0599893, umls-concept:C0682323, umls-concept:C1416904, umls-concept:C1517692, umls-concept:C1522702, umls-concept:C1548789, umls-concept:C1735591, umls-concept:C2936267
pubmed:issue	11
pubmed:dateCreated	2010-10-27
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/M01-RR00064
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101235741
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Cytoskeletal Proteins, http://linkedlifedata.com/resource/pubmed/chemical/LIM Domain Proteins, http://linkedlifedata.com/resource/pubmed/chemical/LPP protein, human
pubmed:status	MEDLINE
pubmed:month	Nov
pubmed:issn	1552-4833
pubmed:author	pubmed-author:ArringtonCammon BCB, pubmed-author:BacinoCarlos ACA, pubmed-author:BowlesNeil ENE, pubmed-author:PatelAnkitaA
pubmed:issnType	Electronic
pubmed:volume	152A
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2919-23
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:20949626-Anal Canal, pubmed-meshheading:20949626-Base Sequence, pubmed-meshheading:20949626-Cytoskeletal Proteins, pubmed-meshheading:20949626-Esophagus, pubmed-meshheading:20949626-Female, pubmed-meshheading:20949626-Gene Dosage, pubmed-meshheading:20949626-Haploinsufficiency, pubmed-meshheading:20949626-Heart Defects, Congenital, pubmed-meshheading:20949626-Humans, pubmed-meshheading:20949626-Infant, pubmed-meshheading:20949626-Introns, pubmed-meshheading:20949626-Kidney, pubmed-meshheading:20949626-LIM Domain Proteins, pubmed-meshheading:20949626-Limb Deformities, Congenital, pubmed-meshheading:20949626-Male, pubmed-meshheading:20949626-Molecular Sequence Data, pubmed-meshheading:20949626-Pedigree, pubmed-meshheading:20949626-Sequence Deletion, pubmed-meshheading:20949626-Spine, pubmed-meshheading:20949626-Tetralogy of Fallot, pubmed-meshheading:20949626-Trachea
pubmed:year	2010
pubmed:articleTitle	Haploinsufficiency of the LIM domain containing preferred translocation partner in lipoma (LPP) gene in patients with tetralogy of Fallot and VACTERL association.
pubmed:affiliation	Division of Cardiology, Department of Pediatrics, University of Utah School of Medicine, Salt Lake City, Utah 84112, USA.
pubmed:publicationType	Journal Article, Case Reports, Research Support, Non-U.S. Gov't, Research Support, N.I.H., Extramural