21290975

Source:http://linkedlifedata.com/resource/pubmed/id/21290975

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0015780, umls-concept:C0021270, umls-concept:C0332597, umls-concept:C0424605, umls-concept:C0796358, umls-concept:C1424876, umls-concept:C1510941, umls-concept:C1515494, umls-concept:C1880022
pubmed:issue	4
pubmed:dateCreated	2011-2-4
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9015261
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:issn	1015-8146
pubmed:author	pubmed-author:ChenC PCP, pubmed-author:ChernS RSR, pubmed-author:LeeC CCC, pubmed-author:PEIM YMY, pubmed-author:RaeA PAP, pubmed-author:TsaiF JFJ, pubmed-author:WantDD, pubmed-author:WuP CPC
pubmed:issnType	Print
pubmed:volume	21
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	457-60
pubmed:meshHeading	pubmed-meshheading:21290975-Abnormalities, Multiple, pubmed-meshheading:21290975-Chromosomes, Human, Pair 9, pubmed-meshheading:21290975-Comparative Genomic Hybridization, pubmed-meshheading:21290975-Developmental Disabilities, pubmed-meshheading:21290975-Female, pubmed-meshheading:21290975-Gene Duplication, pubmed-meshheading:21290975-Humans, pubmed-meshheading:21290975-Infant
pubmed:year	2010
pubmed:articleTitle	A 5.3-Mb duplication of 9p12 --> p13.1 characterized by array CGH in a female infant with developmental delay.
pubmed:publicationType	Letter, Case Reports, Research Support, Non-U.S. Gov't