http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2709761-A1

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filingDate 1993-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_abe3a29fabbcb406d8f5b58272bf3ab4
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publicationDate 1995-03-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber FR-2709761-A1
titleOfInvention Method for detecting molecules containing nucleotide mismatches and for locating these mismatches, and application to the detection of base substitutions or deletions.
abstract Method for detecting and / or localizing mutations or deletions in nucleotide sequences by creating heteroduplexes between two types of double-stranded DNA capable of forming mismatches at the sites of said mutations or deletions. The heteroduplexes are highlighted due to the labeling on each type of strand by different fluorescent molecules or are screened by passage over a support retaining them specifically.
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