137 related articles for article (PubMed ID: 2829363)
21. The distal region of 11p13 and associated genetic diseases.
Mannens M; Hoovers JM; Bleeker-Wagemakers EM; Redeker E; Bliek J; Overbeeke-Melkert M; Saunders G; Williams B; van Heyningen V; Junien C
Genomics; 1991 Oct; 11(2):284-93. PubMed ID: 1769647
[TBL] [Abstract][Full Text] [Related]
22. Long range physical map of the Wilms' tumor-aniridia region on human chromosome 11.
Compton DA; Weil MM; Jones C; Riccardi VM; Strong LC; Saunders GF
Cell; 1988 Dec; 55(5):827-36. PubMed ID: 2847871
[TBL] [Abstract][Full Text] [Related]
23. The T-ALL specific t(11;14)(p13;q11) translocation breakpoint cluster region is located near to the Wilms' tumour predisposition locus.
Boehm T; Lavenir I; Forster A; Wadey RB; Cowell JK; Harbott J; Lampert F; Waters J; Sherrington P; Couillin P
Oncogene; 1988 Dec; 3(6):691-5. PubMed ID: 2577871
[TBL] [Abstract][Full Text] [Related]
24. Characterization of a panel of somatic cell hybrids for subregional mapping along 11p and within band 11p13. Subdivision of the WAGR complex region.
Couillin P; Azoulay M; Henry I; Ravisé N; Grisard MC; Jeanpierre C; Barichard F; Metezeau P; Candelier JJ; Lewis W
Hum Genet; 1989 May; 82(2):171-8. PubMed ID: 2722195
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. Familial aniridia and translocation t(4;11)(q22;p13) without Wilms' tumor.
Simola KO; Knuutila S; Kaitila I; Pirkola A; Pohja P
Hum Genet; 1983; 63(2):158-61. PubMed ID: 6301974
[TBL] [Abstract][Full Text] [Related]
27. Aniridia-Wilms' tumor association: evidence for specific deletion of 11p13.
Francke U; Holmes LB; Atkins L; Riccardi VM
Cytogenet Cell Genet; 1979; 24(3):185-92. PubMed ID: 225131
[TBL] [Abstract][Full Text] [Related]
28. A tumor chromosome rearrangement further defines the 11p13 Wilms tumor locus.
Davis LM; Zabel B; Senger G; Lüdecke HJ; Metzroth B; Call K; Housman D; Claussen U; Horsthemke B; Shows TB
Genomics; 1991 Jul; 10(3):588-92. PubMed ID: 1653761
[TBL] [Abstract][Full Text] [Related]
29. Wilms' tumor-aniridia association: segregation of affected chromosome in somatic cell hybrids, identification of cell surface antigen associated with deleted area, and regional mapping of c-Ha-ras-1 oncogene, insulin gene, and beta-globin gene.
Fisher JH; Miller YE; Sparkes RS; Bateman JB; Kimmel KA; Carey TE; Rodell T; Shoemaker SA; Scoggin CH
Somat Cell Mol Genet; 1984 Sep; 10(5):455-64. PubMed ID: 6089356
[TBL] [Abstract][Full Text] [Related]
30. The chromosome 11 region flanking the t(11;14) breakpoint in human T-ALL is deleted in Wilms' tumor hybrids.
Finver SN; Martiniere C; Kagan J; Cavenee W; Croce CM
Oncogene Res; 1989; 5(2):143-8. PubMed ID: 2558334
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. Molecular analysis of chromosomal rearrangements using pulsed field gel electrophoresis and somatic cell hybrids.
Davis LM
Environ Mol Mutagen; 1991; 18(4):263-9. PubMed ID: 1660807
[TBL] [Abstract][Full Text] [Related]
33. 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]
34. Direct pulsed field gel electrophoresis of Wilms' tumors shows that DNA deletions in 11p13 are rare.
Royer-Pokora B; Ragg S; Heckl-Ostreicher B; Held M; Loos U; Call K; Glaser T; Housman D; Saunders G; Zabel B
Genes Chromosomes Cancer; 1991 Mar; 3(2):89-100. PubMed ID: 1648959
[TBL] [Abstract][Full Text] [Related]
35. A fine-structure deletion map of human chromosome 11p: analysis of J1 series hybrids.
Glaser T; Housman D; Lewis WH; Gerhard D; Jones C
Somat Cell Mol Genet; 1989 Nov; 15(6):477-501. PubMed ID: 2595451
[TBL] [Abstract][Full Text] [Related]
36. Molecular analysis of a reciprocal translocation t(5;11) (q11;p13) in a WAGR patient.
Puissant H; Azoulay M; Serre JL; Piet LL; Junien C
Hum Genet; 1988 Jul; 79(3):280-2. PubMed ID: 2841227
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. c-Ha-ras1 is not deleted in aniridia-Wilms' tumour association.
Huerre C; Despoisse S; Gilgenkrantz S; Lenoir GM; Junien C
Nature; 1983 Oct 13-19; 305(5935):638-41. PubMed ID: 6312328
[TBL] [Abstract][Full Text] [Related]
39. [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]
40. [WAGR syndrome, Wilms' tumor, aniridia, gonadoblastoma, mental retardation: a review apropos of 2 cases].
Mochon MC; Blanc JF; Plauchu H; Philip T
Pediatrie; 1987; 42(4):249-52. PubMed ID: 2823214
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
