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WAGR Syndrome
Known as:
WAGR Complex
, Wilms Tumor-Aniridia-Genitourinary Anomalies-Mental Retardation Syndrome
, Wilms Tumor-Aniridia-Genitourinary Anomalies-MR Syndrome
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A very rare congenital condition involving the complex of Wilms tumor, aniridia, genitourinary abnormalities, and mental retardation. Wilms Tumor…
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National Institutes of Health
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Related topics
Related topics
25 relations
Aniridia
Autosomal dominant inheritance
Chromosome Aberrations
Chromosomes, Human, Pair 11
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Narrower (2)
Chromosome 11p deletion syndrome
Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2008
Highly Cited
2008
ROBO2 gene variants are associated with familial vesicoureteral reflux.
A. Bertoli-Avella
,
M. L. Conte
,
+9 authors
S. Perrotta
Journal of the American Society of Nephrology
2008
Corpus ID: 20107769
The SLIT2 receptor ROBO2 plays a key role in the formation of the ureteric bud, and its inactivation in mice leads to…
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Review
2005
Review
2005
Congenital diaphragmatic hernia in WAGR syndrome
D. Scott
,
M. L. Cooper
,
P. Stankiewicz
,
A. Patel
,
L. Potocki
,
S. Cheung
American Journal of Medical Genetics. Part A
2005
Corpus ID: 30843772
Wilms tumor, aniridia, genitourinary anomalies, and mental retardation (WAGR) syndrome is a contiguous gene deletion syndrome…
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Highly Cited
2001
Highly Cited
2001
Crustal model for the Middle East and North Africa region: implications for the isostatic compensation mechanism
D. Seber
,
E. Sandvol
,
Christine Sandvol
,
Carrie Brindisi
,
M. Barazangi
2001
Corpus ID: 53585104
SUMMARY We present a new 3-D crustal model for the Middle East and North Africa region that includes detailed topography…
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Review
1999
Review
1999
MR imaging of paediatric uterovaginal anomalies
Isla M. Lang
,
P. Babyn
,
G. Oliver
Pediatric Radiology
1999
Corpus ID: 7392471
Background. Transabdominal ultrasound (US) has not proved completely reliable in Müllerian duct anomalies. One study has shown it…
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Highly Cited
1997
Highly Cited
1997
The incidence of PAX6 mutation in patients with simple aniridia: an evaluation of mutation detection in 12 cases.
R. Axton
,
I. Hanson
,
S. Danes
,
G. Sellar
,
V. Heyningen
,
J. Prosser
Journal of Medical Genetics
1997
Corpus ID: 28152971
Twelve aniridia patients, five with a family history and seven presumed to be sporadic, were exhaustively screened in order to…
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Highly Cited
1993
Highly Cited
1993
Aortopexy for Tracheomalacia in Oesophageal Anomalies
Corbally Mt
,
L. Spitz
,
E. Kiely
,
Brereton Rj
,
D. Drake
European journal of pediatric surgery
1993
Corpus ID: 44651295
Forty-eight patients with repaired congenital oesophageal anomaly underwent aortopexy for significant tracheomalacia between 1980…
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Highly Cited
1985
Highly Cited
1985
Breakpoints in the human T-cell antigen receptor α-chain locus in two T-cell leukaemia patients with chromosomal translocations
W. H. Lewis
,
E. E. Michalopoulos
,
DorothyL. Williams
,
M. Minden
,
T. Mak
Nature
1985
Corpus ID: 4334766
Specific chromosomal translocations have been observed in several human and animal tumours and are believed to be important in…
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Review
1984
Review
1984
Del 11p/aniridia complex. Report of three patients and review of 37 observations from the literature
C. Turleau
,
J. Grouchy
,
M. Tournade
,
M. Gagnadoux
,
C. Junien
Clinical Genetics
1984
Corpus ID: 36766240
Three patients (two females, one male) are reported with bilateral aniridia, Wilms' tumor, more or less moderate mental…
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Highly Cited
1983
Highly Cited
1983
The diagnosis of fetal hydrocephalus.
F. Chervenak
,
R. Berkowitz
,
+5 authors
J. Hobbins
American Journal of Obstetrics and Gynecology
1983
Corpus ID: 9330857
Highly Cited
1980
Highly Cited
1980
Regional assignment of catalase (CAT) gene to band 11p13. Association with the aniridia-Wilms' tumor-Gonadoblastoma (WAGR) complex.
C. Junien
,
C. Turleau
,
+4 authors
J. Dufier
Annales de Genetique
1980
Corpus ID: 22485534
A gene dosage effect for catalase (CAT) was investigated in three individuals : one with 11p13 deletion, aniridia, ambiguous…
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