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
|