Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1
pubmed:dateCreated
2008-3-31
pubmed:abstractText
To obtain more insight into the variability of the CFTR mutations found in immigrant cystic fibrosis (CF) patients who are living in Europe now, and to estimate the test sensitivity of different frequently used methods of DNA analysis to detect CF carriers or patients among these Turkish or North African immigrants.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Mar
pubmed:issn
1090-6576
pubmed:author
pubmed:issnType
Print
pubmed:volume
12
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
25-35
pubmed:dateRevised
2009-11-19
pubmed:meshHeading
pubmed-meshheading:18373402-Adolescent, pubmed-meshheading:18373402-Adult, pubmed-meshheading:18373402-Africa, Northern, pubmed-meshheading:18373402-Alleles, pubmed-meshheading:18373402-Child, pubmed-meshheading:18373402-Consanguinity, pubmed-meshheading:18373402-Cystic Fibrosis, pubmed-meshheading:18373402-Cystic Fibrosis Transmembrane Conductance Regulator, pubmed-meshheading:18373402-DNA Mutational Analysis, pubmed-meshheading:18373402-Emigration and Immigration, pubmed-meshheading:18373402-Europe, pubmed-meshheading:18373402-Female, pubmed-meshheading:18373402-Gene Frequency, pubmed-meshheading:18373402-Genetic Testing, pubmed-meshheading:18373402-Heterozygote Detection, pubmed-meshheading:18373402-Homozygote, pubmed-meshheading:18373402-Humans, pubmed-meshheading:18373402-Infant, Newborn, pubmed-meshheading:18373402-Male, pubmed-meshheading:18373402-Mutation, pubmed-meshheading:18373402-Neonatal Screening, pubmed-meshheading:18373402-Parents, pubmed-meshheading:18373402-Questionnaires, pubmed-meshheading:18373402-Sensitivity and Specificity, pubmed-meshheading:18373402-Turkey
pubmed:year
2008
pubmed:articleTitle
CFTR mutations in Turkish and North African cystic fibrosis patients in Europe: implications for screening.
pubmed:affiliation
Department of Clinical Genetics, VU University Medical Center, Amsterdam, The Netherlands. p.lakeman@vumc.nl
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't, Multicenter Study