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Clinical relevance of mutations in the Wilms tumor suppressor 1 gene WT1 and the cadherin-associated protein β1 gene CTNNB1 for patients with Wilms tumors†
Results of long-term surveillance of 71 patients from International Society of Pediatric Oncology Study 9/Society for Pediatric Oncology
Article first published online: 10 JUL 2008
DOI: 10.1002/cncr.23672
Copyright © 2008 American Cancer Society
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How to Cite
Royer-Pokora, B., Weirich, A., Schumacher, V., Uschkereit, C., Beier, M., Leuschner, I., Graf, N., Autschbach, F., Schneider, D. and von Harrach, M. (2008), Clinical relevance of mutations in the Wilms tumor suppressor 1 gene WT1 and the cadherin-associated protein β1 gene CTNNB1 for patients with Wilms tumors. Cancer, 113: 1080–1089. doi: 10.1002/cncr.23672
- †
See editorial on pages 893-6, this issue.
Publication History
- Issue published online: 20 AUG 2008
- Article first published online: 10 JUL 2008
- Manuscript Accepted: 13 FEB 2008
- Manuscript Revised: 11 FEB 2008
- Manuscript Received: 10 OCT 2007
Funded by
- Elterninitiative Kinderkrebsklinik e.V., Duesseldorf
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- 2, , , , , Tumor de Wilms con diferenciación muscular. HistologÃa, inmunofenotipo y análisis molecular de tres casos, Revista Española de PatologÃa, 2012, 45, 2, 67
- 3, Wilms' tumours: about tumour suppressor genes, an oncogene and a chameleon gene, Nature Reviews Cancer, 2011, 11, 2, 111
- 4
- 5, , , , , , Single-Nucleotide Polymorphism in WT1 Gene in a Hyperplastic Intralobar Nephrogenic Rest With Botryoid Protrusion, Urology, 2010, 76, 1, 149
- 6, , , , , , , , Wilms tumor cells with WT1 mutations have characteristic features of mesenchymal stem cells and express molecular markers of paraxial mesoderm, Human Molecular Genetics, 2010, 19, 9, 1651
- 7
- 8, Genetic stratification of Wilms tumor, Cancer, 2008, 113, 5Direct Link:

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