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classificationCPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6876
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 1987-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1991-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_96412a7a30242ad525f17fdc0d0945b3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4eb41e3c3bed52bfe5f918353249a620
publicationDate 1991-06-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-5026837-A
titleOfInvention DNA probe which reveals a hypervariable region on human chromosome 16
abstract A DNA probe p79-2-23 is homologous to at least a portion of a hypervariable DNA region located on chromosome 16q22->q24 in the human genome. The DNA region displays a restriction fragment length polymorphism when digested with certain restriction endonucleases. Unrelated individuals display unique fragment patterns on Southern blots probed with p79-2-23. The probe can be used to produce a genetic "fingerprint" for establishing human identity, determining engraftment of bone marrow transplants, determining parentage, and otherwise mapping genes.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-9966070-A1
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priorityDate 1987-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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