http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2001006780-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6837
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-6837
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 1998-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_76713241e0c7b036bebfe32d6f68a7cc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8c7ab3f1bb2eeff2764b5bfa8037d48f
publicationDate 2001-07-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2001006780-A1
titleOfInvention Process for detecting a known sequence in genomic dna
abstract Described is a process for screening genomic DNA samples for inherited conditions comprising selectively amplifying a portion of the genomic DNA using a primer that is substantially complementary to the portion but may have at least one mismatch nucleotide at or near one end. If the portion is amplified, hybridizing a probe to it, then, attaching the hybridized probe complex to a solid support and detecting the complex, if any.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2010009376-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2006188906-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2022111548-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7670772-B2
priorityDate 1998-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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