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Microarray and kit for diagnosing GCPS syndrome
Microarray and kit for diagnosing GCPS syndrome
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机译:用于诊断GCPS综合征的微阵列和试剂盒
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摘要
PURPOSE: A microarray and a kit for diagnosing GCPS(Greig cephalopolysyndactyly) syndrome are provided to dye a sample with a normal gene copy number and a sample which is suspected to have GCPS syndrome with different fluorescent substances. CONSTITUTION: A microarray and a kit for diagnosing GCPS syndrome contains one or more kinds of genome DNA fragments, 20-100 bp oligonucleotide, 100bp-10kbp cDNA, and one or more kinds of probes. The oligonucleotide is continuously contained in the genome fragment. The cDNA is derived from the genome DNA fragment. The probe is selected from a group consisting of a complement of the genome DNA fragment, oligonucleotide, and cDNA.
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