20202685

Source:http://linkedlifedata.com/resource/pubmed/id/20202685

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0004083, umls-concept:C0020792, umls-concept:C0205419, umls-concept:C1275685, umls-concept:C1707513, umls-concept:C2603343
pubmed:issue	7
pubmed:dateCreated	2010-7-8
pubmed:abstractText	To determine the association of identified copy number variations (CNVs) in whole genome with the risk of Avellino corneal dystrophy (ACD) in a Korean population.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7802443
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Jul
pubmed:issn	1549-4713
pubmed:author	pubmed-author:BaeJoon SeolJS, pubmed-author:CheongHyun SubHS, pubmed-author:ChunJi-YongJY, pubmed-author:KimDong-JoonDJ, pubmed-author:KimEun MiEM, pubmed-author:KimEung KweonEK, pubmed-author:KimJi-OnJO, pubmed-author:LeeEun-JuEJ, pubmed-author:LeeJong-YoungJY, pubmed-author:ParkMieyM, pubmed-author:ParkTae JoonTJ, pubmed-author:ShinHyoung DooHD
pubmed:copyrightInfo	Copyright 2010 American Academy of Ophthalmology. Published by Elsevier Inc. All rights reserved.
pubmed:issnType	Electronic
pubmed:volume	117
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1306-12.e4
pubmed:meshHeading	pubmed-meshheading:20202685-Adolescent, pubmed-meshheading:20202685-Adult, pubmed-meshheading:20202685-Aged, pubmed-meshheading:20202685-Aged, 80 and over, pubmed-meshheading:20202685-Algorithms, pubmed-meshheading:20202685-Asian Continental Ancestry Group, pubmed-meshheading:20202685-Case-Control Studies, pubmed-meshheading:20202685-Child, pubmed-meshheading:20202685-Child, Preschool, pubmed-meshheading:20202685-Corneal Dystrophies, Hereditary, pubmed-meshheading:20202685-DNA Copy Number Variations, pubmed-meshheading:20202685-Female, pubmed-meshheading:20202685-Genome, Human, pubmed-meshheading:20202685-Genome-Wide Association Study, pubmed-meshheading:20202685-Genotype, pubmed-meshheading:20202685-Humans, pubmed-meshheading:20202685-Korea, pubmed-meshheading:20202685-Male, pubmed-meshheading:20202685-Middle Aged, pubmed-meshheading:20202685-Polymorphism, Single Nucleotide, pubmed-meshheading:20202685-Risk Assessment
pubmed:year	2010
pubmed:articleTitle	Identification of genome-wide copy number variations and a family-based association study of Avellino corneal dystrophy.
pubmed:affiliation	Laboratory of Genomic Diversity, Department of Life Science, Sogang University, Shinsu-dong, Mapo-gu, Seoul, Republic of Korea.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't