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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
Additional Information
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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