http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-2171469-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_43a72884e25aaecffebe0942132d704f
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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6858
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6858
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filingDate 1994-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_861df9a764ff8e8457645147373c3aa6
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_63edd9c73b61ebfa4c3e57482bad8be4
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publicationDate 1995-03-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-2171469-A1
titleOfInvention Method for the detection of molecules containing nucleotidic mismatches and location thereof, and application to detection of substitutions of deletions of bases in nucleotidic sequences
abstract Method for detecting and / or localizing mutations or deletions in sequences by creating heteroduplexes between two types of double-stranded DNA capable of forming mismatches at the sites of said mutations or deletions. Heteroduplexes are highlighted by the marking on each type of strand by fluorescent molecules are screened by passage on a support specifically retaining it.
priorityDate 1993-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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