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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Detalles Bibliográficos
Autores principales: Braude, Ilan, Vukovic, Bisera, Prasad, Mona, Marrano, Paula, Turley, Stefanie, Barber, Dwayne, Zielenska, Maria, Squire, Jeremy A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Research Article
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

Internet

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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