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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...
Autores principales: | Braude, Ilan, Vukovic, Bisera, Prasad, Mona, Marrano, Paula, Turley, Stefanie, Barber, Dwayne, Zielenska, Maria, Squire, Jeremy A |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1550726/ https://www.ncbi.nlm.nih.gov/pubmed/16756668 http://dx.doi.org/10.1186/1471-2164-7-138 |
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