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Array CGH Analysis of Paired Blood and Tumor Samples from Patients with Sporadic Wilms Tumor

Array CGH Analysis of Paired Blood and Tumor Samples from Patients with Sporadic Wilms Tumor

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1708567595

Array CGH Analysis of Paired Blood and Tumor Samples from Patients with Sporadic Wilms Tumor

About this item

Full title

Array CGH Analysis of Paired Blood and Tumor Samples from Patients with Sporadic Wilms Tumor

Publisher

United States: Public Library of Science

Journal title

PloS one, 2015-08, Vol.10 (8), p.e0136812-e0136812

Language

English

Formats

Publication information

Publisher

United States: Public Library of Science

More information

Scope and Contents

Contents

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 therapeutic targets. In paired blood and tumor DNA s...

Alternative Titles

Full title

Array CGH Analysis of Paired Blood and Tumor Samples from Patients with Sporadic Wilms Tumor

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_plos_journals_1708567595

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_plos_journals_1708567595

Other Identifiers

ISSN

1932-6203

E-ISSN

1932-6203

DOI

10.1371/journal.pone.0136812

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