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filingDate 2010-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2015-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9722110feb1970be2743d1aa6baf2858
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publicationDate 2015-05-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-9029088-B2
titleOfInvention Human single nucleotide polymorphisms within CODIS loci D13S317, TH01, vWA, D12S391, and D6S1043
abstract Disclosed are methods for human identification utilizing newly discovered single nucleotide polymorphisms (SNPs) within CODIS loci D13S317, TH01, vWA, D12S391 and D6S1043, which can cause allelic dropout. Also disclosed are kits useful in human identification.
priorityDate 2009-10-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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