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filingDate 2005-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_63b3d01bd3ba79bcf599ea16e2ce81db
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8b744b6a55443a5e58305c008cf1d5df
publicationDate 2005-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2568499-A1
titleOfInvention Method of detecting cystic fibrosis associated mutations
abstract The present invention describes a method for the simultaneous identification of two or more single base changes, insertions, deletions or translocations in a plurality of target nucleotide sequences that are markers associated with cystic fibrosis. Multiplex detection is accomplished using multiplexed tagged allele specific primer extension (ASPE) and hybridization of such extended primers to a probe, preferably an addressable anti-tagged support.
priorityDate 2004-06-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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