http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2001299392-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_382ccfc2ebebcaee15aa7cda4cee86bc |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-53 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/G01N33-566 |
| filingDate | 2000-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1fe648b4e5d1a06e5075fdf1fb5fbeeb http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e3a0ea47b265b9eac3db712a0a74a8ed |
| publicationDate | 2001-10-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-2001299392-A |
| titleOfInvention | CATCH22 syndrome detection method |
| abstract | (57) [Summary] [PROBLEMS] To measure CATCH2 expression in a simple, rapid and inexpensive manner compared to the conventional FISH method or CGH method. Provided is a diagnostic technique for the syndrome capable of detecting the two syndromes. A SEQ ID NO: on chromosome 22q11.2 A method for detecting a CATCH22 syndrome, comprising: measuring a polynucleotide sample containing the nucleotide sequence of the exon 12 region of the UFD1L gene sequence represented by No. 1 by a quantitative real-time PCR detection method to detect a defect in the nucleotide sequence; An oligonucleotide used as a probe or primer for the detection. |
| priorityDate | 2000-04-25-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 114.