16275171

Source:http://linkedlifedata.com/resource/pubmed/id/16275171

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0010674, umls-concept:C0026882, umls-concept:C0031437, umls-concept:C0936012
pubmed:issue	1
pubmed:dateCreated	2006-1-27
pubmed:abstractText	Although there are more than 1000 mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, most of them are uncommon and only limited information exists regarding genotype-pulmonary phenotype relationships.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/101128966
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/CFTR protein, human, http://linkedlifedata.com/resource/pubmed/chemical/Cystic Fibrosis Transmembrane..., http://linkedlifedata.com/resource/pubmed/chemical/DNA
pubmed:status	MEDLINE
pubmed:month	Jan
pubmed:issn	1569-1993
pubmed:author	pubmed-author:AudrezetMarie PierreMP, pubmed-author:BraunAndrew TAT, pubmed-author:FarrellPhilip MPM, pubmed-author:FerecClaudeC, pubmed-author:GershanWilliam MWM, pubmed-author:KosorokMichael RMR, pubmed-author:LaxovaAnitaA, pubmed-author:LiZhanhaiZ, pubmed-author:RosenbergMarjorie AMA
pubmed:issnType	Print
pubmed:volume	5
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	33-41
pubmed:dateRevised	2006-11-15
pubmed:meshHeading	pubmed-meshheading:16275171-Child, pubmed-meshheading:16275171-Child, Preschool, pubmed-meshheading:16275171-Chromatography, High Pressure Liquid, pubmed-meshheading:16275171-Cystic Fibrosis, pubmed-meshheading:16275171-Cystic Fibrosis Transmembrane Conductance Regulator, pubmed-meshheading:16275171-DNA, pubmed-meshheading:16275171-Disease Progression, pubmed-meshheading:16275171-Follow-Up Studies, pubmed-meshheading:16275171-Forced Expiratory Volume, pubmed-meshheading:16275171-Genotype, pubmed-meshheading:16275171-Humans, pubmed-meshheading:16275171-Infant, pubmed-meshheading:16275171-Infant, Newborn, pubmed-meshheading:16275171-Phenotype, pubmed-meshheading:16275171-Point Mutation, pubmed-meshheading:16275171-Prognosis, pubmed-meshheading:16275171-Prospective Studies, pubmed-meshheading:16275171-Radiography, Thoracic, pubmed-meshheading:16275171-Severity of Illness Index, pubmed-meshheading:16275171-Spirometry
pubmed:year	2006
pubmed:articleTitle	Cystic fibrosis mutations and genotype-pulmonary phenotype analysis.
pubmed:affiliation	Department of Pediatrics and Biostatistics/Medical Informatics, University of Wisconsin, Madison, WI 53705-2221, USA.
pubmed:publicationType	Journal Article, Comparative Study, Randomized Controlled Trial, Multicenter Study