http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20090112235-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6837
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68
filingDate 2008-04-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_108b3d240cc46f37902627ac0c4c318e
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2d3cf63ac0c2cf6f38ddd9290a334f14
publicationDate 2009-10-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-20090112235-A
titleOfInvention Human chromosome microdeletion analysis chip and idiopathic infertility screening test
abstract The present invention relates to a step, a method and a chip for implementing the same in a high-throughput method to determine the presence or absence of AZFa, AZFb, AZFc region microdeletion of human Y chromosome long arm chromosome. Conventional methods for analyzing Y chromosome deletions, such as karyotyping, Southern blotting, and single polymerase chain reaction (PCR), have low-throughput, low specificity and accuracy. ), A long analysis time is required. Accordingly, the present invention provides multiplex PCR for STS markers and genes capable of comprehensive and specific analysis of AZFa, AZFb, and AZFc microdeletion sites in the chromosome interval 5-6 of human Y chromosome long arm. By incorporating high-specificity probes, we attempt to provide an accurate method for determining idiopathic infertility due to Yq chromosome microdeletion.
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