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Array CGH Analysis of Paired Blood and Tumor Samples from Patients with Sporadic Wilms Tumor
Wilms tumor (WT), the most common cancer of the kidney in infants and children, has a complex etiology that is still poorly understood. Identification of genomic copy number variants (CNV) in tumor genomes provides a better understanding of cancer development which may be useful for diagnosis and th...
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Publicado no: | PLoS One |
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Main Authors: | , , , , , , , , , , , , |
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
Public Library of Science
2015
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Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4552764/ https://ncbi.nlm.nih.gov/pubmed/26317783 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0136812 |
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