Grundy RG - Search Results

1

Perlman and Wiedemann-Beckwith syndromes: two distinct conditions associated with Wilms' tumour.

Grundy RG, Pritchard J, Baraitser M, Risdon A, Robards M. Grundy RG, et al. Eur J Pediatr. 1992 Dec;151(12):895-8. doi: 10.1007/BF01954125. Eur J Pediatr. 1992. PMID: 1361910

2

Ascertainment of the incidence of Beckwith-Wiedemann syndrome in the National Wilms Tumor Study Group.

Grundy R, Pritchard J. Grundy R, et al. J Clin Oncol. 2001 Jan 15;19(2):593-4. doi: 10.1200/JCO.2001.19.2.593. J Clin Oncol. 2001. PMID: 11208855 No abstract available.

3

Loss of heterozygosity for the short arm of chromosome 7 in sporadic Wilms tumour.

Grundy RG, Pritchard J, Scambler P, Cowell JK. Grundy RG, et al. Oncogene. 1998 Jul 23;17(3):395-400. doi: 10.1038/sj.onc.1201927. Oncogene. 1998. PMID: 9690521

4

Loss of heterozygosity on chromosome 16 in sporadic Wilms' tumour.

Grundy RG, Pritchard J, Scambler P, Cowell JK. Grundy RG, et al. Br J Cancer. 1998 Nov;78(9):1181-7. doi: 10.1038/bjc.1998.651. Br J Cancer. 1998. PMID: 9820177 Free PMC article.

5

Familial hepatoblastoma and APC gene mutations: renewed call for molecular research.

Thomas D, Pritchard J, Davidson R, McKiernan P, Grundy RG, de Ville de Goyet J. Thomas D, et al. Among authors: grundy rg. Eur J Cancer. 2003 Oct;39(15):2200-4. doi: 10.1016/s0959-8049(03)00618-x. Eur J Cancer. 2003. PMID: 14522379

6

Outcome of patients with stage III or inoperable WT treated on the second United Kingdom WT protocol (UKWT2); a United Kingdom Children's Cancer Study Group (UKCCSG) study.

Grundy RG, Hutton C, Middleton H, Imeson J, Pritchard J, Kelsey A, Marsden HB, Vujanic GM, Taylor RE; United Kingdom Children's Cancer Study Group. Grundy RG, et al. Pediatr Blood Cancer. 2004 Apr;42(4):311-9. doi: 10.1002/pbc.10477. Pediatr Blood Cancer. 2004. PMID: 14966826 Clinical Trial.

7

Immediate nephrectomy versus preoperative chemotherapy in the management of non-metastatic Wilms' tumour: results of a randomised trial (UKW3) by the UK Children's Cancer Study Group.

Mitchell C, Pritchard-Jones K, Shannon R, Hutton C, Stevens S, Machin D, Imeson J, Kelsey A, Vujanic GM, Gornall P, Walker J, Taylor R, Sartori P, Hale J, Levitt G, Messahel B, Middleton H, Grundy R, Pritchard J; United Kingdom Cancer Study Group. Mitchell C, et al. Eur J Cancer. 2006 Oct;42(15):2554-62. doi: 10.1016/j.ejca.2006.05.026. Epub 2006 Aug 10. Eur J Cancer. 2006. PMID: 16904312 Clinical Trial.

8

Congenital abnormalities and clinical features associated with Wilms' tumour: a comprehensive study from a centre serving a large population.

Ng A, Griffiths A, Cole T, Davison V, Griffiths M, Larkin S, Parkes SE, Mann JR, Grundy RG. Ng A, et al. Among authors: grundy rg. Eur J Cancer. 2007 Jun;43(9):1422-9. doi: 10.1016/j.ejca.2007.03.020. Epub 2007 May 17. Eur J Cancer. 2007. PMID: 17499987

9

Characterization of the breakpoints in unbalanced t(5;11)(p15;p15) constitutional chromosome translocations in two patients with beckwith-wiedemann syndrome using fluorescence in situ hybridisation.

Grundy RG, Aledo R, Cowell JK. Grundy RG, et al. Int J Mol Med. 1998 May;1(5):801-8. doi: 10.3892/ijmm.1.5.801. Int J Mol Med. 1998. PMID: 9852299

10

Molecular subtypes and phenotypic expression of Beckwith-Wiedemann syndrome.

Cooper WN, Luharia A, Evans GA, Raza H, Haire AC, Grundy R, Bowdin SC, Riccio A, Sebastio G, Bliek J, Schofield PN, Reik W, Macdonald F, Maher ER. Cooper WN, et al. Eur J Hum Genet. 2005 Sep;13(9):1025-32. doi: 10.1038/sj.ejhg.5201463. Eur J Hum Genet. 2005. PMID: 15999116

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