| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_431fbdb042f9ad1f81cbb088eb89a671
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_11e74749ae5384f69f15b48477e46c79
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c88ceb051520bb25da4c002e034b6fe7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_268be9afa00cf55b5aa72b1612151ecb
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6e62a5b81a4b4eaaea00341ee903b294
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6050d37ad309abf9f859bd55b945cfea |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q2600-156 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C12Q1-6883 |
| classificationIPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12N15-09 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C12Q1-68 |
| filingDate |
2010-03-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6c21a29b54c746da8adc1aab7133e965
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_db0dba4f4e44a3ee413f3b5c93a118e1
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9556b8cbda484fed1a8cb4f5081ecf3d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9f1c048b05506df95faaba7f4ff42000 |
| publicationDate |
2010-09-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
WO-2010101273-A1 |
| titleOfInvention |
Method for detecting multiple system malformation syndrome accompanied by mental retardation |
| abstract |
In a disease of multiple system malformation syndrome accompanied by mental retardation, the presence or absence of the amplification or deficiency in the human chromosome is analyzed, and the cause of the disease is found. Disclosed is a method for detecting the disease. Specifically, the method can detect multiple system malformation syndrome accompanied by mental retardation by detecting hemizygote deficiency in the region of 3p26.1-3p25.3 in the human chromosome. Preferably, the method is achieved by detecting a signal generated upon the hybridization between a nucleic acid containing a part of the region of 3p26.1-3p25.3 and a nucleic acid analyte on the basis of the hemizygote deficiency in the chromosome region. |
| priorityDate |
2009-03-03-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |