http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-20020023733-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_392d03aa5cd1aa7ee6390d6f5a26a8b8 |
| classificationCPCAdditional | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2563-101 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2531-113 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6837 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6827 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate | 2001-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b99b0342fd051fa751344333804ee454 |
| publicationDate | 2002-03-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | KR-20020023733-A |
| titleOfInvention | Method for diagnosis of congenital adrenal hyperplasia and oligonucleotide chip |
| abstract | The present invention provides a step of preparing an oligonucleotide chip in which a mutation of 21-hydroxylase gene of adrenal syndrome and 7 sets of tandem cDNA fragments of normal genes (exon 1, intron 2, exon 4) are fixed on a solid substrate. ; Amplifying a part of the 21-hydroxylase genomic gene (exon 1, intron 2, exon 4) of the person to be diagnosed by PCR using a primer; Performing hybridization with seven sets of tandem cDNA gene fragments fixed on the amplified gene and oligonucleotide chip; And it relates to a method for diagnosing adrenal gland syndrome comprising the step of searching for the hybridization. |
| priorityDate | 2001-12-13-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 65.