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Large scale copy number variation (CNV) at 14q12 is associated with the presence of genomic abnormalities in neoplasia
BACKGROUND: Advances made in the area of microarray comparative genomic hybridization (aCGH) have enabled the interrogation of the entire genome at a previously unattainable resolution. This has lead to the discovery of a novel class of alternative entities called large-scale copy number variations...
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| Autors principals: | , , , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2006
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1550726/ https://ncbi.nlm.nih.gov/pubmed/16756668 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2164-7-138 |
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