152 related articles for article (PubMed ID: 2841227)
21. Loss of allelic heterozygosity at a second locus on chromosome 11 in sporadic Wilms' tumor cells.
Reeve AE; Sih SA; Raizis AM; Feinberg AP
Mol Cell Biol; 1989 Apr; 9(4):1799-803. PubMed ID: 2542777
[TBL] [Abstract][Full Text] [Related]
22. Balanced reciprocal translocation (X;20) limited to Wilms' tumor in a Wiedemann-Beckwith syndrome.
Diaz de Bustamante A; Delicado A; Garcia de Miguel P; Darnaude MT; de Torres ML; Zumel RM; Lopez Pajares I
Cancer Genet Cytogenet; 1990 Mar; 45(1):35-9. PubMed ID: 2154323
[TBL] [Abstract][Full Text] [Related]
23. Translocation t(5;11)(q13.1;p13) associated with familial isolated aniridia.
Pettenati MJ; Weaver RG; Burton BK
Am J Med Genet; 1989 Oct; 34(2):230-2. PubMed ID: 2817003
[TBL] [Abstract][Full Text] [Related]
24. Correlation of chromosome abnormalities with histological and clinical features in Wilms' and other childhood renal tumors.
Kaneko Y; Homma C; Maseki N; Sakurai M; Hata J
Cancer Res; 1991 Nov; 51(21):5937-42. PubMed ID: 1657374
[TBL] [Abstract][Full Text] [Related]
25. [Hereditary renal tumors: Wilms' tumor--congenital anomalies' syndrome].
Tsuchida Y; Yokomori K; Choi SH
Nihon Rinsho; 1995 Nov; 53(11):2742-8. PubMed ID: 8538037
[TBL] [Abstract][Full Text] [Related]
26. Rapid isolation of moderate and highly polymorphic DNA fragments mapping close to WT (Wilms' tumour) and AN2 (aniridia) on chromosome 11.
Boyd PA; Christie S; Hastie ND; Porteous DJ
Hum Genet; 1989 Mar; 81(4):349-52. PubMed ID: 2564837
[TBL] [Abstract][Full Text] [Related]
27. Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complex.
Junien C; Turleau C; de Grouchy J; Saïd R; Rethoré MO L; Tenconi R; Dufier JL
Ann Genet; 1980; 23(3):165-8. PubMed ID: 6252821
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. WAGR(O?) syndrome and congenital ptosis caused by an unbalanced t(11;15)(p13;p11.2)dn demonstrating a 7 megabase deletion by FISH.
Lennon PA; Scott DA; Lonsdorf D; Wargowski DS; Kirkpatrick S; Patel A; Cheung SW
Am J Med Genet A; 2006 Jun; 140(11):1214-8. PubMed ID: 16646034
[TBL] [Abstract][Full Text] [Related]
30. Complex Chromosomal Rearrangement Involving Chromosomes 10 and 11, Accompanied by Two Adjacent 11p14.1p13 and 11p13p12 Deletions, Identified in a Patient with WAGR Syndrome.
Marakhonov AV; Vasilyeva TA; Minzhenkova ME; Sukhanova NV; Sparber PA; Andreeva NA; Teleshova MV; Baybagisova FK; Shilova NV; Kutsev SI; Zinchenko RA
Int J Mol Sci; 2023 Nov; 24(23):. PubMed ID: 38069245
[TBL] [Abstract][Full Text] [Related]
31. t(11;11)(p13;p15) and high concentration of insulin-like growth factor II in a Wilms' tumor.
Hayashi Y; Hanada R; Yamamoto K; Muchi H
Cancer Genet Cytogenet; 1988 Jul; 33(1):145-7. PubMed ID: 2838157
[No Abstract] [Full Text] [Related]
32. Molecular analysis of aniridia patients for deletions involving the Wilms' tumor gene.
Drechsler M; Meijers-Heijboer EJ; Schneider S; Schurich B; Grond-Ginsbach C; Tariverdian G; Kantner G; Blankenagel A; Kaps D; Schroeder-Kurth T
Hum Genet; 1994 Oct; 94(4):331-8. PubMed ID: 7927324
[TBL] [Abstract][Full Text] [Related]
33. Unbalanced translocation of chromosome 3p in Wilms' tumor.
Walton JM; Lee CL; Mikhail E; Welch JP; Gillis DA
J Pediatr Surg; 1992 Oct; 27(10):1311-4. PubMed ID: 1328583
[TBL] [Abstract][Full Text] [Related]
34. Telomeric fusions in a Wilms' tumor.
Fett-Conte AC; Liedtke Júnior H; Chaves H; Thomé JA; Tajara EH
Cancer Genet Cytogenet; 1993 Sep; 69(2):141-5. PubMed ID: 8402554
[TBL] [Abstract][Full Text] [Related]
35. Molecular mapping and cloning of the breakpoints of a chromosome 11p14.1-p13 deletion associated with the AGR syndrome.
Gessler M; Bruns GA
Genomics; 1988 Aug; 3(2):117-23. PubMed ID: 2852160
[TBL] [Abstract][Full Text] [Related]
36. Unique insertional translocation in a childhood Wilms' tumor survivor detected when his daughter developed bilateral retinoblastoma.
Punnett A; Teshima I; Heon E; Budning A; Sutherland J; Gallie BL; Chan HS
Am J Med Genet A; 2003 Jul; 120A(1):105-9. PubMed ID: 12794701
[TBL] [Abstract][Full Text] [Related]
37. A panel of irradiation-reduced hybrids selectively retaining human chromosome 11p13: their structure and use to purify the WAGR gene complex.
Glaser T; Rose E; Morse H; Housman D; Jones C
Genomics; 1990 Jan; 6(1):48-64. PubMed ID: 2154397
[TBL] [Abstract][Full Text] [Related]
38. Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization.
Fantes JA; Bickmore WA; Fletcher JM; Ballesta F; Hanson IM; van Heyningen V
Am J Hum Genet; 1992 Dec; 51(6):1286-94. PubMed ID: 1334370
[TBL] [Abstract][Full Text] [Related]
39. Wilms' tumor, malformative syndrome, mental retardation and de novo constitutional translocation, t(7;13)(q36;q13).
Bernard JL; Baeteman MA; Mattei JF; Raybaud C; Giraud F
Eur J Pediatr; 1984 Jan; 141(3):175-7. PubMed ID: 6321191
[TBL] [Abstract][Full Text] [Related]
40. Localization of a novel t(1;7) translocation associated with Wilms' tumor predisposition and skeletal abnormalities.
Reynolds PA; Powlesland RM; Keen TJ; Inglehearn CF; Cunningham AF; Green ED; Brown KW
Genes Chromosomes Cancer; 1996 Nov; 17(3):151-5. PubMed ID: 8946193
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
