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4. Nonlinkage of 16q markers to familial predisposition to Wilms' tumor. Huff V; Reeve AE; Leppert M; Strong LC; Douglass EC; Geiser CF; Li FP; Meadows A; Callen DF; Lenoir G Cancer Res; 1992 Nov; 52(21):6117-20. PubMed ID: 1356625 [TBL] [Abstract][Full Text] [Related]
5. Microdissecting the genetic events in nephrogenic rests and Wilms' tumor development. Charles AK; Brown KW; Berry PJ Am J Pathol; 1998 Sep; 153(3):991-1000. PubMed ID: 9736048 [TBL] [Abstract][Full Text] [Related]
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7. Linkage of familial Wilms' tumor predisposition to chromosome 19 and a two-locus model for the etiology of familial tumors. McDonald JM; Douglass EC; Fisher R; Geiser CF; Krill CE; Strong LC; Virshup D; Huff V Cancer Res; 1998 Apr; 58(7):1387-90. PubMed ID: 9537236 [TBL] [Abstract][Full Text] [Related]
8. Prevalence of (Epi)genetic Predisposing Factors in a 5-Year Unselected National Wilms Tumor Cohort: A Comprehensive Clinical and Genomic Characterization. Hol JA; Kuiper RP; van Dijk F; Waanders E; van Peer SE; Koudijs MJ; Bladergroen R; van Reijmersdal SV; Morgado LM; Bliek J; Lombardi MP; Hopman S; Drost J; de Krijger RR; van den Heuvel-Eibrink MM; Jongmans MCJ J Clin Oncol; 2022 Jun; 40(17):1892-1902. PubMed ID: 35230882 [TBL] [Abstract][Full Text] [Related]
9. Nephroblastoma (Wilms' tumor): a model system of aberrant renal development. Re GG; Hazen-Martin DJ; Sens DA; Garvin AJ Semin Diagn Pathol; 1994 May; 11(2):126-35. PubMed ID: 7809506 [TBL] [Abstract][Full Text] [Related]
10. Genetic and epigenetic alterations on the short arm of chromosome 11 are involved in a majority of sporadic Wilms' tumours. Satoh Y; Nakadate H; Nakagawachi T; Higashimoto K; Joh K; Masaki Z; Uozumi J; Kaneko Y; Mukai T; Soejima H Br J Cancer; 2006 Aug; 95(4):541-7. PubMed ID: 16909133 [TBL] [Abstract][Full Text] [Related]
11. Evidence for genetic heterogeneity in familial Wilms' tumor. Huff V; Amos CI; Douglass EC; Fisher R; Geiser CF; Krill CE; Li FP; Strong LC; McDonald JM Cancer Res; 1997 May; 57(10):1859-62. PubMed ID: 9157975 [TBL] [Abstract][Full Text] [Related]
12. Identification of germline DICER1 mutations and loss of heterozygosity in familial Wilms tumour. Palculict TB; Ruteshouser EC; Fan Y; Wang W; Strong L; Huff V J Med Genet; 2016 Jun; 53(6):385-8. PubMed ID: 26566882 [TBL] [Abstract][Full Text] [Related]
13. Germline WT1 mutations in Wilms' tumor patients: preliminary results. Li FP; Breslow NE; Morgan JM; Ghahremani M; Miller GA; Grundy PE; Green DM; Diller LR; Pelletier J Med Pediatr Oncol; 1996 Nov; 27(5):404-7. PubMed ID: 8827066 [TBL] [Abstract][Full Text] [Related]
14. Wilms tumor genetics. Huff V Am J Med Genet; 1998 Oct; 79(4):260-7. PubMed ID: 9781905 [TBL] [Abstract][Full Text] [Related]
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16. A novel WT1 gene mutation associated with wilms' tumor and congenital male genitourinary malformation. Sakamoto J; Takata A; Fukuzawa R; Kikuchi H; Sugiyama M; Kanamori Y; Hashizume K; Hata JI Pediatr Res; 2001 Sep; 50(3):337-44. PubMed ID: 11518820 [TBL] [Abstract][Full Text] [Related]
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18. Loss of heterozygosity at 7p in Wilms' tumour development. Powlesland RM; Charles AK; Malik KT; Reynolds PA; Pires S; Boavida M; Brown KW Br J Cancer; 2000 Jan; 82(2):323-9. PubMed ID: 10646884 [TBL] [Abstract][Full Text] [Related]
19. Genetic and epigenetic features of bilateral Wilms tumor predisposition in patients from the Children's Oncology Group AREN18B5-Q. Murphy AJ; Cheng C; Williams J; Shaw TI; Pinto EM; Dieseldorff-Jones K; Brzezinski J; Renfro LA; Tornwall B; Huff V; Hong AL; Mullen EA; Crompton B; Dome JS; Fernandez CV; Geller JI; Ehrlich PF; Mulder H; Oak N; Maciezsek J; Jablonowski CM; Fleming AM; Pichavaram P; Morton CL; Easton J; Nichols KE; Clay MR; Santiago T; Zhang J; Yang J; Zambetti GP; Wang Z; Davidoff AM; Chen X Nat Commun; 2023 Dec; 14(1):8006. PubMed ID: 38110397 [TBL] [Abstract][Full Text] [Related]
20. Role of the WT1 gene in Wilms' tumour. Haber DA; Housman DE Cancer Surv; 1992; 12():105-17. PubMed ID: 1322241 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]