12865760

Source:http://linkedlifedata.com/resource/pubmed/id/12865760

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008633, umls-concept:C0011155, umls-concept:C0162429, umls-concept:C0175702, umls-concept:C0208973, umls-concept:C0234621, umls-concept:C1415347, umls-concept:C1415349, umls-concept:C1428114, umls-concept:C1517892, umls-concept:C1521638, umls-concept:C1704666, umls-concept:C1709694
pubmed:issue	4
pubmed:dateCreated	2003-7-16
pubmed:abstractText	To identify the relationship between specific genes and phenotypic features of Williams syndrome.
pubmed:grant	http://linkedlifedata.com/resource/pubmed/grant/P01 HD33113
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9815831
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/GTF2I protein, human, http://linkedlifedata.com/resource/pubmed/chemical/GTF2IRD1 protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Muscle Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Nuclear Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Trans-Activators, http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors, TFII
pubmed:status	MEDLINE
pubmed:issn	1098-3600
pubmed:author	pubmed-author:BellugiUrsulaU, pubmed-author:ChenXiao-NingXN, pubmed-author:HirotaHamaoH, pubmed-author:KorenbergJulie RJR, pubmed-author:LincolnAlanA, pubmed-author:MatsuokaRumikoR, pubmed-author:OsawaMakikoM, pubmed-author:RoseFredric EFE, pubmed-author:SalandananLora SLS, pubmed-author:SunaharaMarikoM
pubmed:issnType	Print
pubmed:volume	5
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	311-21
pubmed:dateRevised	2007-11-14
pubmed:meshHeading	pubmed-meshheading:12865760-Adolescent, pubmed-meshheading:12865760-Adult, pubmed-meshheading:12865760-Child, pubmed-meshheading:12865760-Chromosome Mapping, pubmed-meshheading:12865760-Chromosomes, Human, Pair 7, pubmed-meshheading:12865760-Cohort Studies, pubmed-meshheading:12865760-Cosmids, pubmed-meshheading:12865760-Female, pubmed-meshheading:12865760-Gene Deletion, pubmed-meshheading:12865760-Gene Dosage, pubmed-meshheading:12865760-Humans, pubmed-meshheading:12865760-In Situ Hybridization, Fluorescence, pubmed-meshheading:12865760-Intelligence Tests, pubmed-meshheading:12865760-Models, Genetic, pubmed-meshheading:12865760-Muscle Proteins, pubmed-meshheading:12865760-Nuclear Proteins, pubmed-meshheading:12865760-Phenotype, pubmed-meshheading:12865760-Physical Chromosome Mapping, pubmed-meshheading:12865760-Trans-Activators, pubmed-meshheading:12865760-Transcription Factors, TFII, pubmed-meshheading:12865760-Williams Syndrome
pubmed:articleTitle	Williams syndrome deficits in visual spatial processing linked to GTF2IRD1 and GTF2I on chromosome 7q11.23.
pubmed:affiliation	Department of Pediatric Cardiology, Tokyo Women's Medical University, Tokyo, Japan.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S., Case Reports, Research Support, Non-U.S. Gov't