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Array Comparative Genomic Hybridization in Pathology
2008Comparative genomic hybridization (CGH) is a molecular cytogenetic method for the detection and mapping of chromosomal gains and losses.1 It is based on the cohybridization of differentially labeled test and reference DNAs onto metaphase spreads, which usually have been prepared from peripheral blood lymphocytes of a healthy donor. The signal intensity
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[Comparative genomic hybridization(CGH)].
Human cell, 1994A new molecular cytogenetic method, comparative genomic hybridization(CGH), was reviewed. CGH produces a map of DNA sequence copy number on a normal metaphase spread after hybridization with the mixture of tumor DNA and normal reference DNA, which are detected with different fluorochromes, respectively.
M, Matsuta, I, Nishiya
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Array comparative genomic hybridization analysis of uterine leiomyosarcoma
Gynecologic Oncology, 2005Young Lae Cho +2 more
exaly
Array Comparative Genomic Hybridization as a Diagnostic Tool for Syndromic Heart Defects
Journal of Pediatrics, 2010Jeroen Breckpot +2 more
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Diagnostic yield of array comparative genomic hybridization in adults with autism spectrum disorders
Genetics in Medicine, 2014Yajuan J Liu, Liu Yajuan, Hisama Fuki M
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