1 | WAGR
|
| 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
|
2 | ORTHYP1, 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
|
3 | WAGR
|
| 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
|
4 | BDNF, 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
|
5 | PAX6, 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
|
6 | PAX6, 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
|
7 | WAGR
|
| WAGR syndrome: is the 'R' always justified?
|
| Termine C, Parigi G, Rossi M, Romano P, Balottin U.
|
| Clin Dysmorphol 16(1):69-70. 2007
|
8 | WT1, 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
|
9 | WAGR, 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
|
10 | WAGR, 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
|
11 | WAGR, 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
|
12 | WAGR
|
| 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
|
13 | WAGR
|
| 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
|
14 | WAGR
|
| 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
|
15 | WAGR
|
| 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
|
16 | WAGR
|
| 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
|
17 | DDS, 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
|
18 | WAGR
|
| A sequence-ready 3-Mb PAC contig covering 16 breakpoints of the Wilms tumor/aniridia region of human chromosome 11p13.
|
| Niederfhr A, et al.
|
| Genomics 53 : 155-163. 1998
|
19 | WAGR
|
| 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
|
20 | WAGR, 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
|
21 | CAT,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
|
22 | BDNF, 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
|
23 | AN, WT1, WAGR
|
| Molecular analysis of aniridia patients for deletions involving the Wilms' tumor gene.
|
| Drechsler M, et al.
|
| Hum Genet 94 : 331-338. 1994
|
24 | WT1, 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
|
25 | WAGR
|
| 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
|
26 | BDNF, 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
|
27 | WT1, 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
|
28 | WAGR
|
| Submicroscopic deletions at the WAGR locus, revealed by nonradioactive in situ hybridization.
|
| Fantes JA, et al.
|
| Am J Hum Genet 51 : 1286-1294. 1992
|
29 | WT1, 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
|
30 | WAGR, WT1
|
| The distal region of 11p13 and associated genetic diseases.
|
| Mannens M, et al.
|
| Genomics 11 : 284-293. 1991
|
31 | WAGR
|
| 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
|
32 | WAGR
|
| 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
|
33 | WAGR, 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
|
34 | WAGR, GUD
|
| The candidate Wilms' tumour gene is involved in genitourinary development.
|
| Pritchard-Jones K, et al.
|
| Nature 346 : 194-197. 1990
|
35 | WAGR, 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
|
36 | WAGR
|
| Definition of the limits of the Wilms tumor locus on human chromosome 11p13.
|
| Compton DA, et al.
|
| Genomics 6 : 309-315. 1990
|
37 | WAGR, 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
|
38 | WAGR
|
| 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
|
39 | WAGR
|
| 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
|
40 | WAGR
|
| 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
|
41 | WAGR
|
| 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
|
42 | GUD, WAGR
|
| A physical map around the WAGR complex on the short arm of chromosome 11.
|
| Gessler M, et al.
|
| Genomics 5 : 43-55. 1989
|
43 | AN, 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
|
44 | WAGR, D11S156, D11S157
|
| A deletion map of the WAGR region on chromosome 11.
|
| Gessler M, et al.
|
| Am J Hum Genet 44 : 486-495. 1989
|
45 | WAGR
|
| 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
|
46 | WAGR, D11S183
|
| Hitch-hiking from HRAS1 to the WAGR locus with CMGT markers.
|
| Bickmore W, et al.
|
| Nucleic Acids Res 16 : 51-60. 1988
|
47 | D11S89, 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
|
48 | AN, WAGR, D11S93, D11S95
|
| Two anonymous DNA segments distinguish the Wilms' tumor and aniridia loci.
|
| Davis LM, et al.
|
| Science 241 : 840-842. 1988
|
49 | WAGR
|
| Familial predisposition to Wilms' tumour does not map to the short arm of chromosome 11.
|
| Grundy P, et al.
|
| Nature 336 : 374-376. 1988
|
50 | WAGR
|
| Lack of linkage of familial Wilms' tumour to chromosomal band 11p13.
|
| Huff V, et al.
|
| Nature 336 : 377-378. 1988
|
51 | WAGR
|
| 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
|
52 | WAGR, 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
|
53 | WAGR
|
| Chromosome 11, Wilms' tumour and associated congenital diseases.
|
| Mannens M, et al.
|
| (HGM9) Cytogenet Cell Genet 46 : 655. 1987
|
54 | WAGR
|
| 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
|
55 | WAGR
|
| Long-range restriction mapping of 11p13.
|
| Nowak NJ, et al.
|
| (HGM9) Cytogenet Cell Genet 46 : 670. 1987
|
56 | WAGR
|
| Characterization of the aniridia-Wilms' tumor association region of chromosome 11p.
|
| Lewis WH, et al.
|
| (HGM9) Cytogenet Cell Genet 46 : 650. 1987
|
57 | WAGR
|
| 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
|
58 | WAGR, 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
|
59 | WAGR
|
| 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
|
60 | GUD, 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
|
61 | WAGR
|
| Sequences which flanck an 11p deletion observed in an hepatocellular carcinoma map to 11p13.
|
| Fisher JH, et al.
|
| Hum Genet 75 : 66-69. 1987
|
62 | HB-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
|
63 | WAGR
|
| Nonrandom loss of maternal chromosome 11 alleles in Wilms tumors.
|
| Schroeder WT, et al.
|
| Am J Hum Genet 40 : 413-420. 1987
|
64 | WAGR, 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
|
65 | WAGR
|
| The cytogenetics of Wilms' tumor.
|
| Slater RM.
|
| Cancer Genet Cytogenet 19 : 37-41. 1986
|
66 | GUD, 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
|
67 | D11S17, 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
|
68 | CALCA, 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
|
69 | WAGR
|
| Del 11p13/nephroblastoma without aniridia.
|
| Turleau C, et al.
|
| Hum Genet 67 : 455-456. 1984
|
70 | HB-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
|
71 | WAGR
|
| 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
|
72 | WAGR
|
| 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
|
73 | WAGR
|
| Deletion of 11p13 and predisposition to aniridia-Wilms' tumor.
|
| Yunis JJ.
|
| Cytogenet Cell Genet 25 : 220. 1979
|
74 | WAGR
|
| Chromosomal imbalance in the aniridia-Wilms tumor association: 11p interstitial deletion.
|
| Riccardi VM, et al.
|
| Pediatrics 61 : 604-610. 1978
|
75 | WAGR
|
| 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
|
76 | WAGR
|
| 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
|