Functional inactivation of the WTX gene is not a frequent event in Wilms’ tumors

Author:

Perotti D, ,Gamba B,Sardella M,Spreafico F,Terenziani M,Collini P,Pession A,Nantron M,Fossati-Bellani F,Radice P

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Genetics,Molecular Biology

Reference31 articles.

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2. Den Dunnen JT, Antonarakis SE . (2000). Mutation nomenclature extensions and suggestions to describe complex mutations: a discussion. Hum Mutat 15: 7–12.

3. Fukuzawa R, Heathcott RW, More HE, Reeve AE . (2006). Sequential WT1 and CTNNB1 mutations and alterations of {beta}-catenin localisation in intralobar nephrogenic rests and associated Wilms tumours. J Clin Pathol 60: 1013–1016.

4. Grundy PE, Telzerow PE, Breslow N, Moksness J, Huff V, Paterson MC . (1994). Loss of heterozygosity for chromosomes 16q and 1p in Wilms’ tumors predicts an adverse outcome. Cancer Res 54: 2331–2333.

5. Han M, Rivera MN, Batten JM, Haber DA, Cin PD, Iafrate AJ . (2007). Wilms’ tumor with an apparently balanced translocation t(X;18) resulting in deletion of the WTX gene. Genes Chromosomes Cancer 46: 909–913.

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