21183320

Source:http://linkedlifedata.com/resource/pubmed/id/21183320

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0008633, umls-concept:C0010495, umls-concept:C0024779, umls-concept:C0039082, umls-concept:C0205314, umls-concept:C0679622, umls-concept:C1708726, umls-concept:C1744681
pubmed:issue	2
pubmed:dateCreated	2011-1-28
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9011485
pubmed:citationSubset	IM
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	1873-569X
pubmed:author	pubmed-author:AhmadWasimW, pubmed-author:JanIftikhar AhmadIA, pubmed-author:JelaniMusharrafM, pubmed-author:NaeemMuhammadM, pubmed-author:TariqMuhammadM, pubmed-author:UllahHazratH
pubmed:issnType	Electronic
pubmed:volume	61
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	134-6
pubmed:meshHeading	pubmed-meshheading:21183320-Adolescent, pubmed-meshheading:21183320-Child, pubmed-meshheading:21183320-Child, Preschool, pubmed-meshheading:21183320-Chromosomes, Human, Pair 9, pubmed-meshheading:21183320-Cutis Laxa, pubmed-meshheading:21183320-Genotype, pubmed-meshheading:21183320-Humans, pubmed-meshheading:21183320-Infant, pubmed-meshheading:21183320-Pedigree, pubmed-meshheading:21183320-Polymorphism, Single Nucleotide, pubmed-meshheading:21183320-Sequence Analysis, DNA
pubmed:year	2011
pubmed:articleTitle	Congenital cutis laxa syndrome maps to a novel locus on chromosome 9q13-q21.32.
pubmed:publicationType	Letter, Research Support, Non-U.S. Gov't