 Comparative Genomic Hybridization
"Comparative Genomic Hybridization" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
A method for comparing two sets of chromosomal DNA by analyzing differences in the copy number and location of specific sequences. It is used to look for large sequence changes such as deletions, duplications, amplifications, or translocations.
| Descriptor ID |
D055028
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| MeSH Number(s) |
E05.393.285.240 E05.393.520.500 E05.393.661.187
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| Concept/Terms |
Comparative Genomic Hybridization- Comparative Genomic Hybridization
- Comparative Genomic Hybridizations
- Genomic Hybridization, Comparative
- Genomic Hybridizations, Comparative
- Hybridization, Comparative Genomic
- Hybridizations, Comparative Genomic
- Comparative Genome Hybridization
- Comparative Genome Hybridizations
- Genome Hybridization, Comparative
- Genome Hybridizations, Comparative
- Hybridization, Comparative Genome
- Hybridizations, Comparative Genome
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Below are MeSH descriptors whose meaning is more general than "Comparative Genomic Hybridization".
Below are MeSH descriptors whose meaning is more specific than "Comparative Genomic Hybridization".
This graph shows the total number of publications written about "Comparative Genomic Hybridization" by people in this website by year, and whether "Comparative Genomic Hybridization" was a major or minor topic of these publications.
To see the data from this visualization as text, click here.
| Year | Major Topic | Minor Topic | Total |
|---|
| 2010 | 2 | 1 | 3 | | 2011 | 0 | 1 | 1 | | 2012 | 0 | 2 | 2 | | 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Comparative Genomic Hybridization" by people in Profiles.
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Li W, Cooley LD, August KJ, Richardson AI, Shao L, Ahmed AA, Farooqi MS, Zwick DL. Cuplike nuclear morphology is highly associated with IKZF1 deletion in pediatric precursor B-cell ALL. Blood. 2019 07 18; 134(3):324-329.
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Abdelmoity AT, LePichon JB, Nyp SS, Soden SE, Daniel CA, Yu S. 15q11.2 proximal imbalances associated with a diverse array of neuropsychiatric disorders and mild dysmorphic features. J Dev Behav Pediatr. 2012 Sep; 33(7):570-6.
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Pastuszak AW, Lamb DJ. The genetics of male fertility--from basic science to clinical evaluation. J Androl. 2012 Nov-Dec; 33(6):1075-84.
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Jorgez CJ, Weedin JW, Sahin A, Tannour-Louet M, Han S, Bournat JC, Mielnik A, Cheung SW, Nangia AK, Schlegel PN, Lipshultz LI, Lamb DJ. Aberrations in pseudoautosomal regions (PARs) found in infertile men with Y-chromosome microdeletions. J Clin Endocrinol Metab. 2011 Apr; 96(4):E674-9.
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Lepichon JB, Bittel DC, Graf WD, Yu S. A 15q13.3 homozygous microdeletion associated with a severe neurodevelopmental disorder suggests putative functions of the TRPM1, CHRNA7, and other homozygously deleted genes. Am J Med Genet A. 2010 May; 152A(5):1300-4.
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Graf WD, Le Pichon JB, Bittel DC, Abdelmoity AT, Yu S. Practice parameter: evaluation of the child with microcephaly (an evidence-based review): report of the quality standards subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society. Neurology. 2010 Mar 30; 74(13):1080-1; author reply 1081.
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Rush ET, Schaefer GB. Identification of an X-linked deletion syndrome through comparative genomic hybridization microarray. Semin Pediatr Neurol. 2010 Mar; 17(1):51-3.
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Butler MG, Bittel DC, Kibiryeva N, Cooley LD, Yu S. An interstitial 15q11-q14 deletion: expanded Prader-Willi syndrome phenotype. Am J Med Genet A. 2010 Feb; 152A(2):404-8.
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Yu S, Kielt M, Stegner AL, Kibiryeva N, Bittel DC, Cooley LD. Quantitative real-time polymerase chain reaction for the verification of genomic imbalances detected by microarray-based comparative genomic hybridization. Genet Test Mol Biomarkers. 2009 Dec; 13(6):751-60.
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Yu S, Bittel DC, Kibiryeva N, Zwick DL, Cooley LD. Validation of the Agilent 244K oligonucleotide array-based comparative genomic hybridization platform for clinical cytogenetic diagnosis. Am J Clin Pathol. 2009 Sep; 132(3):349-60.
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