Hol JA, Jongmans MCJ, Sudour-Bonnange H, Ramirez-Villar GL, Chowdhury T, Rechnitzer C, Pal N, Schleiermacher G, Karow A, Kuiper RP, De Camargo B, Avcin S, Redzic D, Wachtel A, Segers H, Vujanic GM, Van Tinteren H, Bergeron C, Pritchard-Jones K, Graf N, Van Den Heuvel-Eibrink MM (2020)
Publication Type: Journal article
Publication year: 2020
DOI: 10.1002/cncr.33304
Background WAGR syndrome (Wilms tumor, aniridia, genitourinary anomalies, and range of developmental delays) is a rare contiguous gene deletion syndrome with a 45% to 60% risk of developing Wilms tumor (WT). Currently, surveillance and treatment recommendations are based on limited evidence.
APA:
Hol, J.A., Jongmans, M.C.J., Sudour-Bonnange, H., Ramirez-Villar, G.L., Chowdhury, T., Rechnitzer, C.,... Van Den Heuvel-Eibrink, M.M. (2020). Clinical characteristics and outcomes of children with WAGR syndrome and Wilms tumor and/or nephroblastomatosis: The 30-year SIOP-RTSG experience. Cancer. https://dx.doi.org/10.1002/cncr.33304
MLA:
Hol, Janna A., et al. "Clinical characteristics and outcomes of children with WAGR syndrome and Wilms tumor and/or nephroblastomatosis: The 30-year SIOP-RTSG experience." Cancer (2020).
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