172 related articles for article (PubMed ID: 11920832)
1. 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]
2. 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]
3. 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]
4. 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]
5. 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]
6. [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]
7. 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]
8. 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]
9. Evaluation of chromosome 11p imbalances in aniridia and Wilms tumor patients.
Busch M; Leube B; Thiel A; Schanze I; Beier M; Royer-Pokora B
Am J Med Genet A; 2013 May; 161A(5):958-64. PubMed ID: 23494989
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. 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]
12. A rare case of an isolated PAX6 mutation, aniridia, and Wilms tumor.
Lind KT; Cost NG; Zegar K; Kuldanek SA; Enzenauer RW; Schneider KW
Ophthalmic Genet; 2021 Apr; 42(2):216-217. PubMed ID: 33300417
[No Abstract] [Full Text] [Related]
13. Genetic analysis of chromosome 11p13 and the PAX6 gene in a series of 125 cases referred with aniridia.
Robinson DO; Howarth RJ; Williamson KA; van Heyningen V; Beal SJ; Crolla JA
Am J Med Genet A; 2008 Mar; 146A(5):558-69. PubMed ID: 18241071
[TBL] [Abstract][Full Text] [Related]
14. PAX6 3' deletion in a family with aniridia.
Wawrocka A; Budny B; Debicki S; Jamsheer A; Sowinska A; Krawczynski MR
Ophthalmic Genet; 2012 Mar; 33(1):44-8. PubMed ID: 21985185
[TBL] [Abstract][Full Text] [Related]
15. [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]
16. 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]
17. De novo chromosome translocation t (2; 11) (p25.1; p13) in a patient with aniridia and genitourinary abnormalities.
Hung HM; Lin SC; Su PH; Chen JY
Acta Paediatr Taiwan; 2003; 44(2):101-3. PubMed ID: 12845852
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 11p13 deletions can be more frequent than the PAX6 gene point mutations in Polish patients with aniridia.
Wawrocka A; Sikora A; Kuszel L; Krawczynski MR
J Appl Genet; 2013 Aug; 54(3):345-51. PubMed ID: 23761016
[TBL] [Abstract][Full Text] [Related]
20. A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.
Crolla JA; Cawdery JE; Oley CA; Young ID; Gray J; Fantes J; van Heyningen V
J Med Genet; 1997 Mar; 34(3):207-12. PubMed ID: 9132491
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
