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8081395
Source:
http://linkedlifedata.com/resource/pubmed/id/8081395
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41
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Statements in which the resource exists as a subject.
Predicate
Object
rdf:type
pubmed:Citation
lifeskim:mentions
umls-concept:C0015295
,
umls-concept:C0017362
,
umls-concept:C0056889
,
umls-concept:C0599155
pubmed:issue
4
pubmed:dateCreated
1994-10-10
pubmed:language
eng
pubmed:journal
http://linkedlifedata.com/resource/pubmed/journal/9215429
pubmed:citationSubset
IM
pubmed:chemical
http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers
pubmed:status
MEDLINE
pubmed:issn
1059-7794
pubmed:author
pubmed-author:BeldjordCC
,
pubmed-author:BienvenuTT
,
pubmed-author:KaplanJ CJC
,
pubmed-author:PetitpretzPP
pubmed:issnType
Print
pubmed:volume
3
pubmed:geneSymbol
CFTR
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
395-6
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:8081395-Adult
,
pubmed-meshheading:8081395-Base Sequence
,
pubmed-meshheading:8081395-Cystic Fibrosis
,
pubmed-meshheading:8081395-DNA Mutational Analysis
,
pubmed-meshheading:8081395-DNA Primers
,
pubmed-meshheading:8081395-Electrophoresis, Polyacrylamide Gel
,
pubmed-meshheading:8081395-Female
,
pubmed-meshheading:8081395-Genes, Regulator
,
pubmed-meshheading:8081395-Humans
,
pubmed-meshheading:8081395-Molecular Sequence Data
,
pubmed-meshheading:8081395-Nucleic Acid Denaturation
,
pubmed-meshheading:8081395-Point Mutation
pubmed:year
1994
pubmed:articleTitle
A missense mutation (F87L) in exon 3 of the cystic fibrosis transmembrane conductance regulator gene.
pubmed:affiliation
Laboratoire de Biochimie Génétique, Hôpital Cochin, Paris, France.
pubmed:publicationType
Journal Article
,
Research Support, Non-U.S. Gov't