153 related articles for article (PubMed ID: 9192846)
1. The reticulocalbin gene maps to the WAGR region in human and to the Small eye Harwell deletion in mouse.
Kent J; Lee M; Schedl A; Boyle S; Fantes J; Powell M; Rushmere N; Abbott C; van Heyningen V; Bickmore WA
Genomics; 1997 Jun; 42(2):260-7. PubMed ID: 9192846
[TBL] [Abstract][Full Text] [Related]
2. Polymerase chain reaction-based risk assessment for Wilms tumor in sporadic aniridia.
Gupta SK; De Becker I; Guernsey DL; Neumann PE
Am J Ophthalmol; 1998 May; 125(5):687-92. PubMed ID: 9625553
[TBL] [Abstract][Full Text] [Related]
3. Raised risk of Wilms tumour in patients with aniridia and submicroscopic WT1 deletion.
van Heyningen V; Hoovers JM; de Kraker J; Crolla JA
J Med Genet; 2007 Dec; 44(12):787-90. PubMed ID: 17630404
[TBL] [Abstract][Full Text] [Related]
4. Congenital diaphragmatic hernia in WAGR syndrome.
Scott DA; Cooper ML; Stankiewicz P; Patel A; Potocki L; Cheung SW
Am J Med Genet A; 2005 May; 134(4):430-3. PubMed ID: 15779010
[TBL] [Abstract][Full Text] [Related]
5. Population-based risk estimates of Wilms tumor in sporadic aniridia. A comprehensive mutation screening procedure of PAX6 identifies 80% of mutations in aniridia.
Grønskov K; Olsen JH; Sand A; Pedersen W; Carlsen N; Bak Jylling AM; Lyngbye T; Brøndum-Nielsen K; Rosenberg T
Hum Genet; 2001 Jul; 109(1):11-8. PubMed ID: 11479730
[TBL] [Abstract][Full Text] [Related]
6. WAGR syndrome--a case report.
Mahale A; Poornima V; Shrestha M
Nepal Med Coll J; 2007 Jun; 9(2):138-40. PubMed ID: 17899969
[TBL] [Abstract][Full Text] [Related]
7. Prediction by FISH analysis of the occurrence of Wilms tumor in aniridia patients.
Muto R; Yamamori S; Ohashi H; Osawa M
Am J Med Genet; 2002 Apr; 108(4):285-9. PubMed ID: 11920832
[TBL] [Abstract][Full Text] [Related]
8. Three patients with hallucal polydactyly and WAGR syndrome, including discordant expression of Wilms tumor in MZ twins.
Brémond-Gignac D; Gérard-Blanluet M; Copin H; Bitoun P; Baumann C; Crolla JA; Benzacken B; Verloes A
Am J Med Genet A; 2005 May; 134(4):422-5. PubMed ID: 15779023
[TBL] [Abstract][Full Text] [Related]
9. [Molecular genetic study of the PAX6 gene in aniridia patients].
Wolf M; Zabel B; Lorenz B; Blankenagel A; Ghorbani MB; Schwenn O; Wildhardt G
Ophthalmologe; 1998 Dec; 95(12):828-30. PubMed ID: 10025146
[TBL] [Abstract][Full Text] [Related]
10. The Wilms tumour (WT1) gene is mutated in a secondary leukaemia in a WAGR patient.
Pritchard-Jones K; Renshaw J; King-Underwood L
Hum Mol Genet; 1994 Sep; 3(9):1633-7. PubMed ID: 7833922
[TBL] [Abstract][Full Text] [Related]
11. Frequent chromosome aberrations revealed by molecular cytogenetic studies in patients with aniridia.
Crolla JA; van Heyningen V
Am J Hum Genet; 2002 Nov; 71(5):1138-49. PubMed ID: 12386836
[TBL] [Abstract][Full Text] [Related]
12. A 556 kb deletion in the downstream region of the PAX6 gene causes familial aniridia and other eye anomalies in a Chinese family.
Cheng F; Song W; Kang Y; Yu S; Yuan H
Mol Vis; 2011 Feb; 17():448-55. PubMed ID: 21321669
[TBL] [Abstract][Full Text] [Related]
13. A familial pericentric inversion of chromosome 11 associated with a microdeletion of 163 kb and microduplication of 288 kb at 11p13 and 11q22.3 without aniridia or eye anomalies.
Balay L; Totten E; Okada L; Zell S; Ticho B; Israel J; Kogan J
Am J Med Genet A; 2016 Jan; 170A(1):202-9. PubMed ID: 26419218
[TBL] [Abstract][Full Text] [Related]
14. [Two neonates with congenital aniridia: the necessity of genetic investigation].
van Os E; Niemarkt HJ; Verreussel MJ; Cruysberg JR; Bok LA; Spruijt L
Ned Tijdschr Geneeskd; 2008 Mar; 152(10):569-73. PubMed ID: 18402324
[TBL] [Abstract][Full Text] [Related]
15. Inactivation of the remaining allele of the WT1 gene in a Wilms' tumour from a WAGR patient.
Brown KW; Watson JE; Poirier V; Mott MG; Berry PJ; Maitland NJ
Oncogene; 1992 Apr; 7(4):763-8. PubMed ID: 1314370
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Mutation in the PAX6 gene in twenty patients with aniridia.
Chao LY; Huff V; Strong LC; Saunders GF
Hum Mutat; 2000; 15(4):332-9. PubMed ID: 10737978
[TBL] [Abstract][Full Text] [Related]
18. A deletion map of the WAGR region on chromosome 11.
Gessler M; Thomas GH; Couillin P; Junien C; McGillivray BC; Hayden M; Jaschek G; Bruns GA
Am J Hum Genet; 1989 Apr; 44(4):486-95. PubMed ID: 2539014
[TBL] [Abstract][Full Text] [Related]
19. A submicroscopic deletion of 11p13 associated with the WAGR syndrome.
Nanclares GP; Martínez F; Bilbao JR; Navajas A; Martínez R; López-Arístegui MA; Castaño L
Clin Genet; 2003 Apr; 63(4):319-22. PubMed ID: 12702167
[No Abstract] [Full Text] [Related]
20. Complete sequencing of the Fugu WAGR region from WT1 to PAX6: dramatic compaction and conservation of synteny with human chromosome 11p13.
Miles C; Elgar G; Coles E; Kleinjan DJ; van Heyningen V; Hastie N
Proc Natl Acad Sci U S A; 1998 Oct; 95(22):13068-72. PubMed ID: 9789042
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
