16941003

Source:http://linkedlifedata.com/resource/pubmed/id/16941003

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0012634, umls-concept:C0205422, umls-concept:C0599883, umls-concept:C2717924
pubmed:issue	9
pubmed:dateCreated	2006-8-30
pubmed:commentsCorrections	http://linkedlifedata.com/resource/pubmed/commentcorrection/16941003-16906162, http://linkedlifedata.com/resource/pubmed/commentcorrection/16941003-16906163, http://linkedlifedata.com/resource/pubmed/commentcorrection/16941003-16906164, http://linkedlifedata.com/resource/pubmed/commentcorrection/16941003-16940994
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9216904
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA, http://linkedlifedata.com/resource/pubmed/chemical/Genetic Markers
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	1061-4036
pubmed:author	pubmed-author:LupskiJames RJR
pubmed:issnType	Print
pubmed:volume	38
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	974-6
pubmed:dateRevised	2011-11-17
pubmed:meshHeading	pubmed-meshheading:16941003-Chromosome Breakage, pubmed-meshheading:16941003-Chromosome Inversion, pubmed-meshheading:16941003-Chromosomes, Human, Pair 17, pubmed-meshheading:16941003-Cohort Studies, pubmed-meshheading:16941003-DNA, pubmed-meshheading:16941003-Databases, Genetic, pubmed-meshheading:16941003-Gene Deletion, pubmed-meshheading:16941003-Gene Dosage, pubmed-meshheading:16941003-Gene Duplication, pubmed-meshheading:16941003-Gene Rearrangement, pubmed-meshheading:16941003-Genetic Diseases, Inborn, pubmed-meshheading:16941003-Genetic Markers, pubmed-meshheading:16941003-Genetic Testing, pubmed-meshheading:16941003-Genetic Variation, pubmed-meshheading:16941003-Genome, Human, pubmed-meshheading:16941003-Haplotypes, pubmed-meshheading:16941003-Humans, pubmed-meshheading:16941003-Intellectual Disability, pubmed-meshheading:16941003-Nucleic Acid Hybridization, pubmed-meshheading:16941003-Polymorphism, Genetic, pubmed-meshheading:16941003-Recombination, Genetic
pubmed:year	2006
pubmed:articleTitle	Genome structural variation and sporadic disease traits.
pubmed:publicationType	Comparative Study, Comment, News