133 related articles for article (PubMed ID: 1676905)
1. Microdissection of chromosome band 11p15.5: characterization of probes mapping distal to the HBBC locus.
Newsham I; Claussen U; Lüdecke HJ; Mason M; Senger G; Horsthemke B; Cavenee W
Genes Chromosomes Cancer; 1991 Mar; 3(2):108-16. PubMed ID: 1676905
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Familial Wiedemann-Beckwith syndrome and a second Wilms tumor locus both map to 11p15.5.
Koufos A; Grundy P; Morgan K; Aleck KA; Hadro T; Lampkin BC; Kalbakji A; Cavenee WK
Am J Hum Genet; 1989 May; 44(5):711-9. PubMed ID: 2539717
[TBL] [Abstract][Full Text] [Related]
5. 11p15.5-specific libraries for identification of potential gene sequences involved in Beckwith-Wiedemann syndrome and tumorigenesis.
Puech A; Ahnine L; Lüdecke HJ; Senger G; Ivens A; Jeanpierre C; Little P; Horsthemke B; Claussen U; Jones C
Genomics; 1992 Aug; 13(4):1274-80. PubMed ID: 1380484
[TBL] [Abstract][Full Text] [Related]
6. A radiation hybrid map of the distal short arm of human chromosome 11, containing the Beckwith-Wiedemann and associated embryonal tumor disease loci.
Richard CW; Boehnke M; Berg DJ; Lichy JH; Meeker TC; Hauser E; Myers RM; Cox DR
Am J Hum Genet; 1993 May; 52(5):915-21. PubMed ID: 8387721
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. Multiple genetic abnormalities of 11p15 in Wilms' tumor.
Feinberg AP
Med Pediatr Oncol; 1996 Nov; 27(5):484-9. PubMed ID: 8827078
[TBL] [Abstract][Full Text] [Related]
9. Molecular nature of genetic changes resulting in loss of heterozygosity of chromosome 11 in Wilms' tumours.
Mannens M; Slater RM; Heyting C; Bliek J; de Kraker J; Coad N; de Pagter-Holthuizen P; Pearson PL
Hum Genet; 1988 Dec; 81(1):41-8. PubMed ID: 2848758
[TBL] [Abstract][Full Text] [Related]
10. Parental imprinting of human chromosome region 11p15.3-pter involved in the Beckwith-Wiedemann syndrome and various human neoplasia.
Mannens M; Hoovers JM; Redeker E; Verjaal M; Feinberg AP; Little P; Boavida M; Coad N; Steenman M; Bliek J
Eur J Hum Genet; 1994; 2(1):3-23. PubMed ID: 7913866
[TBL] [Abstract][Full Text] [Related]
11. Regional localization of DNA probes on the short arm of chromosome 11 using aniridia-Wilms' tumor-associated deletions.
Mannens M; Slater RM; Heyting C; Geurts van Kessel A; Goedde-Salz E; Frants RR; Van Ommen GJ; Pearson PL
Hum Genet; 1987 Feb; 75(2):180-7. PubMed ID: 3028933
[TBL] [Abstract][Full Text] [Related]
12. Cytogenetics and molecular genetics of Wilms' tumor of childhood.
Slater RM; Mannens MM
Cancer Genet Cytogenet; 1992 Jul; 61(2):111-21. PubMed ID: 1322233
[TBL] [Abstract][Full Text] [Related]
13. Beck-Wiedemann syndrome and Wilms' tumour.
Ward A
Mol Hum Reprod; 1997 Feb; 3(2):157-68. PubMed ID: 9239720
[TBL] [Abstract][Full Text] [Related]
14. Physical mapping of 3 candidate tumor suppressor genes relative to Beckwith-Wiedemann syndrome associated chromosomal breakpoints at 11p15.3.
Redeker E; Alders M; Hoovers JM; Richard CW; Westerveld A; Mannens M
Cytogenet Cell Genet; 1995; 68(3-4):222-5. PubMed ID: 7842740
[TBL] [Abstract][Full Text] [Related]
15. Excess functional copy of allele at chromosomal region 11p15 may cause Wiedemann-Beckwith (EMG) syndrome.
Kubota T; Saitoh S; Matsumoto T; Narahara K; Fukushima Y; Jinno Y; Niikawa N
Am J Med Genet; 1994 Feb; 49(4):378-83. PubMed ID: 7909196
[TBL] [Abstract][Full Text] [Related]
16. Genomic imprinting of p57KIP2, a cyclin-dependent kinase inhibitor, in mouse.
Hatada I; Mukai T
Nat Genet; 1995 Oct; 11(2):204-6. PubMed ID: 7550351
[TBL] [Abstract][Full Text] [Related]
17. Molecular sublocalization and characterization of the 11;22 translocation breakpoint in a malignant rhabdoid tumor.
Newsham I; Daub D; Besnard-Guerin C; Cavenee W
Genomics; 1994 Feb; 19(3):433-40. PubMed ID: 8188285
[TBL] [Abstract][Full Text] [Related]
18. Novel transcribed sequences within the BWS/WT2 region in 11p15.5: tissue-specific expression correlates with cancer type.
Crider-Miller SJ; Reid LH; Higgins MJ; Nowak NJ; Shows TB; Futreal PA; Weissman BE
Genomics; 1997 Dec; 46(3):355-63. PubMed ID: 9441738
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. 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]
[Next] [New Search]
