http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2013163935-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12N15-10
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6806
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 2013-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_89bb585e5e4a218815c7ea347111afa6
publicationDate 2013-11-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-2013163935-A1
titleOfInvention Method for isolating and obtaining pure and complete fetus genome dna
abstract Provided is a method for isolating and obtaining pure and complete fetus genome DNA, comprising the following steps: isolating a nucleated erythrocyte from the maternal (pregnant woman) peripheral blood, identifying the individual hereditary feature subtype of the mother and/or father of the fetus; conducting high fidelity whole genome DNA amplification on the signal cell isolated from the nucleated erythrocyte; identifying the individual hereditary feature subtype of the fetus according to the laws of hereditary, and determining a fetus-originating genome DNA. The fetus-originating pure whole genome DNA provided by the present invention lays a material foundation for prenatal heredity diagnosis.
priorityDate 2012-05-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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