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3. A developmental context for multiple genetic alterations in Wilms' tumor. Feinberg AP J Cell Sci Suppl; 1994; 18():7-12. PubMed ID: 7883796 [TBL] [Abstract][Full Text] [Related]
4. A common region of loss of heterozygosity in Wilms' tumor and embryonal rhabdomyosarcoma distal to the D11S988 locus on chromosome 11p15.5. Besnard-Guérin C; Newsham I; Winqvist R; Cavenee WK Hum Genet; 1996 Feb; 97(2):163-70. PubMed ID: 8566947 [TBL] [Abstract][Full Text] [Related]
5. Role of genomic imprinting in Wilms' tumour and overgrowth disorders. Reeve AE Med Pediatr Oncol; 1996 Nov; 27(5):470-5. PubMed ID: 8827076 [TBL] [Abstract][Full Text] [Related]
10. Human KVLQT1 gene shows tissue-specific imprinting and encompasses Beckwith-Wiedemann syndrome chromosomal rearrangements. Lee MP; Hu RJ; Johnson LA; Feinberg AP Nat Genet; 1997 Feb; 15(2):181-5. PubMed ID: 9020845 [TBL] [Abstract][Full Text] [Related]
11. Microdeletion of target sites for insulator protein CTCF in a chromosome 11p15 imprinting center in Beckwith-Wiedemann syndrome and Wilms' tumor. Prawitt D; Enklaar T; Gärtner-Rupprecht B; Spangenberg C; Oswald M; Lausch E; Schmidtke P; Reutzel D; Fees S; Lucito R; Korzon M; Brozek I; Limon J; Housman DE; Pelletier J; Zabel B Proc Natl Acad Sci U S A; 2005 Mar; 102(11):4085-90. PubMed ID: 15743916 [TBL] [Abstract][Full Text] [Related]
12. A constitutional BWS-related t(11;16) chromosome translocation occurring in the same region of chromosome 16 implicated in Wilms' tumors. Newsham I; Kindler-Röhrborn A; Daub D; Cavenee W Genes Chromosomes Cancer; 1995 Jan; 12(1):1-7. PubMed ID: 7534105 [TBL] [Abstract][Full Text] [Related]
13. Coding mutations in p57KIP2 are present in some cases of Beckwith-Wiedemann syndrome but are rare or absent in Wilms tumors. O'Keefe D; Dao D; Zhao L; Sanderson R; Warburton D; Weiss L; Anyane-Yeboa K; Tycko B Am J Hum Genet; 1997 Aug; 61(2):295-303. PubMed ID: 9311733 [TBL] [Abstract][Full Text] [Related]
15. [Wilms' tumors and malformation complexes]. Hata J; Fukuzawa R; Takata A; Kikuchi H Nihon Rinsho; 2000 Jul; 58(7):1419-25. PubMed ID: 10921316 [TBL] [Abstract][Full Text] [Related]
16. An overview of the clinical and molecular genetics of Wilms' tumor. Grundy P; Coppes M Med Pediatr Oncol; 1996 Nov; 27(5):394-7. PubMed ID: 8827064 [No Abstract] [Full Text] [Related]
17. The M1 subunit of ribonucleotide reductase refines mapping of genetic rearrangements at chromosome 11p15. Byrne JA; Little MH; Smith PJ Cancer Genet Cytogenet; 1992 Apr; 59(2):206-9. PubMed ID: 1316226 [TBL] [Abstract][Full Text] [Related]
20. Beckwith-Wiedemann syndrome. Weksberg R; Shuman C; Smith AC Am J Med Genet C Semin Med Genet; 2005 Aug; 137C(1):12-23. PubMed ID: 16010676 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]