The DOI matches its Crossref record; 61 of the 61 references it cites were found in a registry or an index.
Genomic microarrays in human genetic disease and cancer
Open accessAbstract
Alterations in the genome that lead to changes in DNA sequence copy number are a characteristic of solid tumors and are found in association with developmental abnormalities and/or mental retardation. Comparative genomic hybridization (CGH) can be used to detect and map these changes. Recent improvements in the resolution and sensitivity of CGH have been possible through implementation of microarray-based CGH (array CGH). Here we discuss the performance characteristics of different array platforms and review some of the recent applications of array CGH in cancer and medical genetics.
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Cites
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Cited by
Detection of large-scale variation in the human genome
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Genetic studies in intellectual disability and related disorders
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Array comparative genomic hybridization and its applications in cancer
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Metadata
- Authors
- Albertson, D. G., & Pinkel, D.
- Venue
- Human Molecular Genetics
- Publisher
- Oxford University Press (OUP)
- Published
- 2003-08-05
- Volume
- 12
- Issue
- suppl 2
- Pages
- R145-R152
- ISSN
- 0964-6906 (ISSN-L)
- 1460-2083
- OpenAlex
- W2119317141
- Cited by
- 371
- References
- 61
- FWCI
- 24.45
- Type
- journal article
- Language
- en
- Open access
- bronze
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