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Localization of a novel t(1;7) translocation associated with Wilms' tumor predisposition and skeletal abnormalities.
Genes Chromosomes Cancer. 1996 Nov;17(3):151-5. doi: 10.1002/(SICI)1098-2264(199611)17:3<151::AID-GCC2>3.0.CO;2-3.
Genes Chromosomes Cancer. 1996.
PMID: 8946193
The parathyroid hormone-responsive B1 gene is interrupted by a t(1;7)(q42;p15) breakpoint associated with Wilms' tumour.
Vernon EG, Malik K, Reynolds P, Powlesland R, Dallosso AR, Jackson S, Henthorn K, Green ED, Brown KW.
Vernon EG, et al.
Oncogene. 2003 Mar 6;22(9):1371-80. doi: 10.1038/sj.onc.1206332.
Oncogene. 2003.
PMID: 12618763
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Loss of heterozygosity at 7p in Wilms' tumour development.
Powlesland RM, Charles AK, Malik KT, Reynolds PA, Pires S, Boavida M, Brown KW.
Powlesland RM, et al.
Br J Cancer. 2000 Jan;82(2):323-9. doi: 10.1054/bjoc.1999.0922.
Br J Cancer. 2000.
PMID: 10646884
Free PMC article.
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Transactivation of the WT1 antisense promoter is unique to the WT1[+/-] isoform.
Moorwood K, Salpekar A, Ivins SM, Hall J, Powlesland RM, Brown KW, Malik K.
Moorwood K, et al. Among authors: powlesland rm.
FEBS Lett. 1999 Jul 30;456(1):131-6. doi: 10.1016/s0014-5793(99)00944-8.
FEBS Lett. 1999.
PMID: 10452544
Free article.
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