Citations for
1WAGR
Deletion and duplication of 11p13-11p14: Reciprocal aberrations derived from a paternal insertion.
Dolan M, Berry SA, Rubin KR, Hirsch B.
Am J Med Genet A 155(11):2775-83. doi: 10.1002/ajmg.a.34232. Epub 2011 Sep 19. 2011
2DBH, WAGR
Mosaic deletion 11p13 in a child with dopamine beta-hydroxylase deficiency-Case report and review of the literature.
Erez A, Li J, Geraghty MT, Ben-Shachar S, Cooper ML, Mensing DE, Vonalt KD, Ou Z, Pursley AN, Chinault AC, Patel A, Cheung SW, Sahoo T.
Am J Med Genet A 152A(3):732-6.PMID: 20186791 2010
3WAGR
Array-CGH analysis in a patient with WAGR syndrome and a reciprocal translocation t(2;11) inherited from the normal father with double translocation.
Gimelli S, Divizia MT, Lerone M, Bricco L, Béna F, Antonarakis SE, Ravazzolo R, Gimelli G.
Am J Med Genet A 152A(8):2130-3. No abstract available. PMID: 20635368 2010
4BDNF, WAGR, WAGRO
Brain-derived neurotrophic factor and obesity in the WAGR syndrome.
Han JC, Liu QR, Jones M, Levinn RL, Menzie CM, Jefferson-George KS, Adler-Wailes DC, Sanford EL, Lacbawan FL, Uhl GR, Rennert OM, Yanovski JA.
N Engl J Med 359(9):918-27. Erratum in: N Engl J Med. 2008 Sep 25;359(13):1414. 2008
5PAX6, AN, WAGR
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 146(5):558-69. 2008
6PAX6, AN, WAGR
Pax6 3' deletion results in aniridia, autism and mental retardation.
Davis LK, Meyer KJ, Rudd DS, Librant AL, Epping EA, Sheffield VC, Wassink TH.
Hum Genet 123(4):371-8. Epub 2008 Mar 6. Review. 2008
7WAGR
WAGR syndrome: is the 'R' always justified?
Termine C, Parigi G, Rossi M, Romano P, Balottin U.
Clin Dysmorphol 16(1):69-70. 2007
8WT1, WT1, WAGR
A CTCF-binding silencer regulates the imprinted genes AWT1 and WT1-AS and exhibits sequential epigenetic defects during Wilms' tumourigenesis.
Hancock AL, Brown KW, Moorwood K, Moon H, Holmgren C, Mardikar SH, Dallosso AR, Klenova E, Loukinov D, Ohlsson R, Lobanenkov VV, Malik K.
Hum Mol Genet 16(3):343-54. Epub 2007 Jan 8. 2007
9WAGR, WT1
Complete sex reversal in a WAGR syndrome patient.
Le Caignec C, Delnatte C, Vermeesch JR, Boceno M, Joubert M, Lavenant F, David A, Rival JM.
Am J Med Genet A 143(22):2692-5. 2007
10WAGR, WT1, AN
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 44(12):787-90. Epub 2007 Jul 14. 2007
11WAGR, PAX6, WT1
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 140(11):1214-8. 2006
12WAGR
Congenital diaphragmatic hernia in WAGR syndrome.
Scott DA, Cooper ML, Stankiewicz P, Patel A, Potocki L, Cheung SW.
Am J Med Genet A 134(4):430-3. Review. 2005
13WAGR
WAGR syndrome: a clinical review of 54 cases.
Fischbach BV, Trout KL, Lewis J, Luis CA, Sika M.
Pediatrics 116(4):984-8. Review. 2005
14WAGR
Frequent chromosome aberrations revealed by molecular cytogenetic studies in patients with aniridia.
Crolla JA, van Heyningen V.
Am J Hum Genet 71(5):1138-49. Epub 2002 Oct 17. 2002
15WAGR
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 108(4):285-9. 2002
16WAGR
Renal failure in the Denys-Drash and Wilms' tumor-aniridia syndromes.
Breslow NE, Takashima JR, Ritchey ML, Strong LC, Green DM.
Cancer Res 60(15):4030-2. 2000
17DDS, WAGR
Bilateral Wilms tumor in a boy with severe hypospadias and cryptochidism due to a heterozygous mutation in the WT1 gene.
Kohler B, et al.
Pediatr Res 45(2):187-90. 1999
18WAGR
A sequence-ready 3-Mb PAC contig covering 16 breakpoints of the Wilms tumor/aniridia region of human chromosome 11p13.
NiederfŸhr A, et al.
Genomics 53 : 155-163. 1998
19WAGR
A FISH approach to defining the extent and possible clinical significance of deletions at the WAGR locus.
Crolla JA, et al.
J Med Genet 34 : 207-212. 1997
20WAGR, EXT2
WAGR syndrome and multiple exostoses in a patient with del(11)(p11.2p14.2).
McGaughran JM, et al.
J Med Genet 32 : 823-824. 1995
21CAT,CD59,FSHB,KCNA4,WAGR
An integrated YAC clone contig for the WAGR region on human chromosome 11p13-p14.1.
Gawin B, et al.
Genomics 30 : 37-45. 1995
22BDNF, FSHB, GTF2H1, MYOD1, WAGR
A high-resolution integrated physical, cytogenetic, and genetic map of human chromosome 11 : distal p13 to proximal p15.1.
Fantes JA, et al.
Genomics 25 : 447-461. 1995
23AN, WT1, WAGR
Molecular analysis of aniridia patients for deletions involving the Wilms' tumor gene.
Drechsler M, et al.
Hum Genet 94 : 331-338. 1994
24WT1, WAGR
The Wilms tumour (WT1) gene is mutated in a secondary leukaemia in a WAGR patient.
Pritchard-Jones K, et al.
Hum Mol Genet 3 : 1633-1637. 1994
25WAGR
An unusual cystic lesion histologically similar to autosomal dominant polycystic kidney disease in a child with aniridia and del 11p13.
Schvimer M, et al.
J Urol 152 : 1218-1220. 1994
26BDNF, WAGR
A 1.7-Mb YAC contig around the human BDNF gene (11p13) : integration of the physical, genetic, and cytogenetic maps in relation to WAGR syndrome.
Rosier MF, et al.
Genomics 24 : 69-77. 1994
27WT1, WAGR
Homozygous inactivation of WTI in a Wilms' tumor associated with the WAGR syndrome.
Gessler M, et al.
Genes Chromosomes Cancer 7 : 131-136. 1993
28WAGR
Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization.
Fantes JA, et al.
Am J Hum Genet 51 : 1286-1294. 1992
29WT1, WAGR
Inactivation of the remaining allele of the WT1 gene in a Wilms' tumour from a WAGR patient.
Brown KW, et al.
Oncogene 7 : 763-768. 1992
30WAGR, WT1
The distal region of 11p13 and associated genetic diseases.
Mannens M, et al.
Genomics 11 : 284-293. 1991
31WAGR
A gene and breakpoint anchored map of the WAGR deletion region of human chromosome 11p.
Bruns G, et al.
(HGM11) Cytogenet Cell Genet 58 : 1956. 1991
32WAGR
A panel of irradiation-reduced hybrids selectively retaining human chromosome 11p13: their structure and use to purify the WAGR gene complex.
Glaser T, et al.
Genomics 6 : 48-64. 1990
33WAGR, WT1
Constitutional and somatic deletions of two different regions of maternal chromosome 11 in Wilms tumor.
Jeanpierre C, et al.
Genomics 7 : 434-438. 1990
34WAGR, GUD
The candidate Wilms' tumour gene is involved in genitourinary development.
Pritchard-Jones K, et al.
Nature 346 : 194-197. 1990
35WAGR, GUD
Role for the Wilms tumor gene in genital development?
van Heyningen V, et al.
Proc Natl Acad Sci U S A 87 : 5383-5386. 1990
36WAGR
Definition of the limits of the Wilms tumor locus on human chromosome 11p13.
Compton DA, et al.
Genomics 6 : 309-315. 1990
37WAGR, AN
Rapid isolation of moderate and highly poymorphic DNA fragments mapping close to WT (Wilms' tumour) and AN2 (aniridia) on chromosome 11.
Boyd PA, et al.
Hum Genet 81 : 349-352. 1989
38WAGR
Molecular definition of de novo and genetically transmitted WAGR-associated rearrangements of 11p13.
Lavedan C, Barichard F, Azoulay M, Couillin P, Molina Gomez D, Nicolas H, Quack B, Rethore MO, Noel B, Junien C.
Cytogenet Cell Genet 50 : 70-74. 1989
39WAGR
The aniridia-Wilms' tumour association : molecular and genetic analysis of chromosome deletions on the short arm of chromosome 11.
Cowell JK, Wadey RB, Buckle BB, Pritchard J.
Hum Genet 82 : 123-126. 1989
40WAGR
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, Ravise N, Grisard MC, Jeanpierre C, Barichard F, Metezeau P, Candelier JJ, Lewis W, et al.
Hum Genet 82 : 171-178. 1989
41WAGR
A highly polymorphic locus cloned from the breakpoint of a chromosome 11p13 deletion associated with the WAGR syndrome.
Glaser T, et al.
Genomics 5 : 880-893. 1989
42GUD, WAGR
A physical map around the WAGR complex on the short arm of chromosome 11.
Gessler M, et al.
Genomics 5 : 43-55. 1989
43AN, WAGR
CpG islands surround a DNA segment located between translocation breakpoints associated with genitourinary dysplasia and aniridia.
Bickmore WA, et al.
Genomics 5 : 685-693. 1989
44WAGR, D11S156, D11S157
A deletion map of the WAGR region on chromosome 11.
Gessler M, et al.
Am J Hum Genet 44 : 486-495. 1989
45WAGR
Analysis of WAGR deletions and related translocations with gene-specific DNA probes, using FACS-selected cell hybrids.
Seawright A, et al.
Somat Cell Mol Genet 14 : 21-30. 1988
46WAGR, D11S183
Hitch-hiking from HRAS1 to the WAGR locus with CMGT markers.
Bickmore W, et al.
Nucleic Acids Res 16 : 51-60. 1988
47D11S89, D11S90, D11S93, D11S95, WAGR
Four new DNA markers are assigned to the WAGR region of 11p13 : isolation and regional assignment of 112 chromosome 11 anonymous DNA segments.
Davis LM, et al.
Genomics 3 : 264-271. 1988
48AN, WAGR, D11S93, D11S95
Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci.
Davis LM, et al.
Science 241 : 840-842. 1988
49WAGR
Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11.
Grundy P, et al.
Nature 336 : 374-376. 1988
50WAGR
Lack of linkage of familial Wilms' tumour to chromosomal band 11p13.
Huff V, et al.
Nature 336 : 377-378. 1988
51WAGR
Molecular mapping and cloning of the breakpoints of a chromosome 11p14.1-p13 deletion associated with the AGR syndrome.
Gessler M, et al.
Genomics 3 : 117-123. 1988
52WAGR, GUD
Analysis of WAGR deletions and related translocations with gene-specific DNA probes using somatic cell hybrids.
van Heyningen V, et al.
(HGM9) Cytogenet Cell Genet 46 : 708. 1987
53WAGR
Chromosome 11, Wilms' tumour and associated congenital diseases.
Mannens M, et al.
(HGM9) Cytogenet Cell Genet 46 : 655. 1987
54WAGR
Analysis of human chromosome 11 by pulsed field gel electrophoresis using markers which flank the WAGR locus.
Bickmore W, et al.
(HGM9) Cytogenet Cell Genet 46 : 581. 1987
55WAGR
Long-range restriction mapping of 11p13.
Nowak NJ, et al.
(HGM9) Cytogenet Cell Genet 46 : 670. 1987
56WAGR
Characterization of the aniridia-Wilms' tumor association region of chromosome 11p.
Lewis WH, et al.
(HGM9) Cytogenet Cell Genet 46 : 650. 1987
57WAGR
Mapping the WAGR region of chromosome 11p : somatic cell hybrids provide a fine structure genetic map.
Glaser TM, et al.
(HGM9) Cytogenet Cell Genet 46 : 620. 1987
58WAGR, D11S152, D11S153, D11S154, D11S155, D11S156, D11S157
DNA probes for chromosome 11 and the WAGR deletion.
Bruns GAP, et al.
(HGM9) Cytogenet Cell Genet 46 : 588. 1987
59WAGR
Mitotic recombination with loss of heterozygosity distal to FSHB in a WAGR associated nephroblastoma.
Henry I, et al.
(HGM9) Cytogenet Cell Genet 46 : 628. 1987
60GUD, WAGR
HRAS1-selected chromosome transfer generates markers that colocalize aniridia- and genitourinary dysplasia-associated translocation breakpoints and the Wilms tumor gene within band 11p13.
Porteous DJ, et al.
Proc Natl Acad Sci U S A 84 : 5355-5359. 1987
61WAGR
Sequences which flanck an 11p deletion observed in an hepatocellular carcinoma map to 11p13.
Fisher JH, et al.
Hum Genet 75 : 66-69. 1987
62HB-NA@, HBB, HBBP1, HBD, HBE1, HBG1, HBG2, WAGR
Regional localization of DNA probes on the short arm of chromosome 11 using aniridia-Wilms' tumor-associated deletions.
Mannens M, et al.
Hum Genet 75 : 180-187. 1987
63WAGR
Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors.
Schroeder WT, et al.
Am J Hum Genet 40 : 413-420. 1987
64WAGR, AN
Familial isolated aniridia associated with a translocation involving chromosomes 11 and 22 [t(11;22)(p13;q12.2)].
Moore JW, et al.
Hum Genet 72 : 297-302. 1986
65WAGR
The cytogenetics of Wilms' tumor.
Slater RM.
Cancer Genet Cytogenet 19 : 37-41. 1986
66GUD, WAGR
Male pseudohermaphroditism, partial androgen receptors defect, 11p13 deletion : indication of gene localization.
Malpuech G, et al.
Am J Med Genet 24 : 679-684. 1986
67D11S17, D11S18, D11S20, D11S24, WAGR
The beta-subunit of follicle-stimulating hormone is deleted in patients with aniridia and Wilms' tumour, allowing a further definition of the WAGR locus.
Glaser T, et al.
Nature 321 : 882-887. 1986
68CALCA, CAT, WAGR
Molecular analysis of chromosome 11 deletions in aniridia-Wilms tumor syndrome.
Van Heyningen V, et al.
Proc Natl Acad Sci U S A 82 : 8592-8596. 1985
69WAGR
Del 11p13/nephroblastoma without aniridia.
Turleau C, et al.
Hum Genet 67 : 455-456. 1984
70HB-NA@, INS, WAGR, HRAS
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, et al.
Somat Cell Mol Genet 10 : 455-464. 1984
71WAGR
Del 11p/aniridia complex. Report of three patients and review of 37 observations from the literature.
Turleau C, de Grouchy J, Tournade MF, Gagnadoux MF, Junien C.
Clin Genet 26(4):356-62. 1984
72WAGR
Del11p13/nephroblastoma without aniridia.
Turleau C, de Grouchy J, Nihoul-Fekete C, Dufier JL, Chavin-Colin F, Junien C.
Hum Genet 67(4):455-6. 1984
73WAGR
Deletion of 11p13 and predisposition to aniridia-Wilms' tumor.
Yunis JJ.
Cytogenet Cell Genet 25 : 220. 1979
74WAGR
Chromosomal imbalance in the aniridia-Wilms tumor association: 11p interstitial deletion.
Riccardi VM, et al.
Pediatrics 61 : 604-610. 1978
75WAGR
Chromosomal imbalance in the Aniridia-Wilms' tumor association: 11p interstitial deletion.
Riccardi VM, Sujansky E, Smith AC, Francke U.
Pediatrics 61(4):604-10. 1978
76WAGR
Association of Wilms's tumor with aniridia, hemihypertrophy and other congenital malformations.
Miller RW, Fraumeni JF Jr, Manning MD.
N Engl J Med 270:922-7. No abstract available. 1964