15017334

Source:http://linkedlifedata.com/resource/pubmed/id/15017334

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0010674, umls-concept:C0019425, umls-concept:C0026882, umls-concept:C0237401, umls-concept:C0376249
pubmed:issue	2
pubmed:dateCreated	2004-3-12
pubmed:abstractText	To determine the carrier frequency of the 3199del6 cystic fibrosis (CF) mutation in individuals heterozygous for I148T in a large-scale CF testing population.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9815831
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers
pubmed:status	MEDLINE
pubmed:issn	1098-3600
pubmed:author	pubmed-author:BullerArleneA, pubmed-author:ChenRebeccaR, pubmed-author:HantashFerasF, pubmed-author:OlsonSusanS, pubmed-author:RedmanJoy BJB, pubmed-author:StromCharles MCM
pubmed:issnType	Print
pubmed:volume	6
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	108-9
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:15017334-Base Sequence, pubmed-meshheading:15017334-Cystic Fibrosis, pubmed-meshheading:15017334-DNA Primers, pubmed-meshheading:15017334-Genotype, pubmed-meshheading:15017334-Heterozygote, pubmed-meshheading:15017334-Humans, pubmed-meshheading:15017334-Mutation, Missense, pubmed-meshheading:15017334-Sequence Analysis, DNA, pubmed-meshheading:15017334-Sequence Deletion
pubmed:articleTitle	Frequency of the cystic fibrosis 3199del6 mutation in individuals heterozygous for I148T.
pubmed:affiliation	Molecular Genetics Department, Nichols Institute, Quest Diagnostics, San Juan Capistrano, California 92690, USA.
pubmed:publicationType	Journal Article, Comparative Study