Allele loss at 16q defines poorer prognosis Wilms tumour irrespective of treatment approach in the UKW1–3 clinical trials: A Children’s Cancer and Leukaemia Group (CCLG) study

Author:

Messahel Boo,Williams Richard,Ridolfi Antonia,A’Hern Roger,Warren William,Tinworth Lorna,Hobson Rachel,Al-Saadi Reem,Whyman Gavin,Brundler Marie-Anne,Kelsey Anna,Sebire Neil,Jones Chris,Vujanic Gordan,Pritchard-Jones Kathy

Publisher

Elsevier BV

Subject

Cancer Research,Oncology

Reference21 articles.

1. The treatment of stages I–IV favorable histology Wilms’ tumor;Green;J Clin Oncol,2004

2. The genetics of Wilms tumour – a case of disrupted development;Hastie;Ann Rev Genet,1994

3. Allele loss in Wilms tumors of chromosome arms 11q, 16q, and 22q correlate with clinicopathological parameters;Klamt;Genes Chromosomes Cancer,1998

4. Loss of heterozygosity for chromosomes 16q and 1p in Wilms’ tumors predicts an adverse outcome;Grundy;Cancer Res,1994

5. Loss of heterozygosity on chromosome 16 in sporadic Wilms’ tumour;Grundy;Brit J Cancer,1998

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