118 related articles for article (PubMed ID: 7865265)
1. Analysis of paediatric tumour types associated with hemihyperplasia in childhood.
Smith PJ; Sullivan M; Algar E; Shapiro DN
J Paediatr Child Health; 1994 Dec; 30(6):515-7. PubMed ID: 7865265
[TBL] [Abstract][Full Text] [Related]
2. 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]
3. 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]
4. Diagnostic criteria and tumor screening for individuals with isolated hemihyperplasia.
Clericuzio CL; Martin RA
Genet Med; 2009 Mar; 11(3):220-2. PubMed ID: 19367194
[TBL] [Abstract][Full Text] [Related]
5. Molecular genetic basis of Wilms' tumour?
Cole TR
Br J Cancer; 1995 Feb; 71(2):427. PubMed ID: 7710515
[No Abstract] [Full Text] [Related]
6. Analysis of the methylation status of the KCNQ1OT and H19 genes in leukocyte DNA for the diagnosis and prognosis of Beckwith-Wiedemann syndrome.
Gaston V; Le Bouc Y; Soupre V; Burglen L; Donadieu J; Oro H; Audry G; Vazquez MP; Gicquel C
Eur J Hum Genet; 2001 Jun; 9(6):409-18. PubMed ID: 11436121
[TBL] [Abstract][Full Text] [Related]
7. 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]
8. 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]
9. Simultaneous Presentation of Wilms Tumor and Immature Ovarian Teratoma in Beckwith-Wiedemann Syndrome.
White JC; Liu J; Nahar A
J Pediatr Hematol Oncol; 2018 Jan; 40(1):e61-e63. PubMed ID: 28692553
[TBL] [Abstract][Full Text] [Related]
10. Molecular genetics of Wilms' tumour.
Tay JS
J Paediatr Child Health; 1995 Oct; 31(5):379-83. PubMed ID: 8554853
[TBL] [Abstract][Full Text] [Related]
11. Nephroblastomatosis or Wilms tumor in a fourth patient with a somatic PIK3CA mutation.
Gripp KW; Baker L; Kandula V; Conard K; Scavina M; Napoli JA; Griffin GC; Thacker M; Knox RG; Clark GR; Parker VE; Semple R; Mirzaa G; Keppler-Noreuil KM
Am J Med Genet A; 2016 Oct; 170(10):2559-69. PubMed ID: 27191687
[TBL] [Abstract][Full Text] [Related]
12. Wiedemann-Beckwith syndrome and chromosomal duplication 4q/deficiency 18p.
Fryns JP; Kleczkowska A; Devriendt K; Devliegher H; Van den Berghe H
Genet Couns; 1993; 4(1):37-41. PubMed ID: 8471219
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. Comparative genomic hybridization analysis of hepatoblastomas: additional evidence for a genetic link with Wilms tumor and rhabdomyosarcoma.
Steenman M; Tomlinson G; Westerveld A; Mannens M
Cytogenet Cell Genet; 1999; 86(2):157-61. PubMed ID: 10545709
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Genetics of paediatric solid tumours.
Cowell JK
Br Med Bull; 1994 Jul; 50(3):600-23. PubMed ID: 7987643
[TBL] [Abstract][Full Text] [Related]
17. Proportion of cells with paternal 11p15 uniparental disomy correlates with organ enlargement in Wiedemann-beckwith syndrome.
Itoh N; Becroft DM; Reeve AE; Morison IM
Am J Med Genet; 2000 May; 92(2):111-6. PubMed ID: 10797434
[TBL] [Abstract][Full Text] [Related]
18. Beckwith-Wiedemann syndrome.
Norman AM; Read AP; Donnai D
J Med Genet; 1992 Sep; 29(9):679. PubMed ID: 1404305
[No Abstract] [Full Text] [Related]
19. [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]
20. Cytogenetic abnormalities in mesoblastic nephroma: a link to Wilms' tumour?
Roberts P; Lockwood LR; Lewis IJ; Bailey CC; Batcup G; Williams J
Med Pediatr Oncol; 1993; 21(6):416-20. PubMed ID: 8390601
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]