Review on WAGR (Wilms' tumor/aniridia/genitourinary anomalies/mental retardation syndrome), with data on clinics, and the genes involved
The WAGR contiguous gene deletion syndrome is a combination of Wilms tumor, Aniridia, Genito-urinary...
OBJECTIVE: The aim of this study was to determine if there is a significant difference in the risk o...
Wilms' tumour is an embryonic kidney tumour thought to arise through aberrant mesenchymal stem cell ...
Congenital anomaly syndrome consisting of Wilms tumor, aniridia, genitourinary malformations and men...
The constitutional chromosomal deletion within the short arm of one copy of chromosome 11, at band p...
Inheritance: Generally sporadic, a few inherited cases sometimes with milder phenotype were reported...
Seventy-seven patients with aniridia, referred for cytogenetic analysis predominantly to assess Wilm...
Review on WT1 (Wilms' tumor suppressor gene), with data on DNA, on the protein encoded, and where th...
BACKGROUND: WAGR syndrome (Wilms tumor, aniridia, genitourinary anomalies, and range of developmenta...
Conventional cytogenetic studies on a female infant with sporadic aniridia revealed what appeared to...
Review on Kidney: Nephroblastoma (Wilms tumor), with data on clinics, and the genes involved
Review on Waardenburg syndrome (WS), with data on clinics, and the genes involved
Wilm's tumour, aniridia, genitourinary abnormalities, and mental retardation (WAGR) syndrome is a ra...
Wilms' tumor is a childhood nephroblastoma that is postulated to arise through the inactivation of a...
Nephroblastoma (Wilms tumor – WT) is the most common kidney tumor among the pediatric population, fi...
The WAGR contiguous gene deletion syndrome is a combination of Wilms tumor, Aniridia, Genito-urinary...
OBJECTIVE: The aim of this study was to determine if there is a significant difference in the risk o...
Wilms' tumour is an embryonic kidney tumour thought to arise through aberrant mesenchymal stem cell ...
Congenital anomaly syndrome consisting of Wilms tumor, aniridia, genitourinary malformations and men...
The constitutional chromosomal deletion within the short arm of one copy of chromosome 11, at band p...
Inheritance: Generally sporadic, a few inherited cases sometimes with milder phenotype were reported...
Seventy-seven patients with aniridia, referred for cytogenetic analysis predominantly to assess Wilm...
Review on WT1 (Wilms' tumor suppressor gene), with data on DNA, on the protein encoded, and where th...
BACKGROUND: WAGR syndrome (Wilms tumor, aniridia, genitourinary anomalies, and range of developmenta...
Conventional cytogenetic studies on a female infant with sporadic aniridia revealed what appeared to...
Review on Kidney: Nephroblastoma (Wilms tumor), with data on clinics, and the genes involved
Review on Waardenburg syndrome (WS), with data on clinics, and the genes involved
Wilm's tumour, aniridia, genitourinary abnormalities, and mental retardation (WAGR) syndrome is a ra...
Wilms' tumor is a childhood nephroblastoma that is postulated to arise through the inactivation of a...
Nephroblastoma (Wilms tumor – WT) is the most common kidney tumor among the pediatric population, fi...
The WAGR contiguous gene deletion syndrome is a combination of Wilms tumor, Aniridia, Genito-urinary...
OBJECTIVE: The aim of this study was to determine if there is a significant difference in the risk o...
Wilms' tumour is an embryonic kidney tumour thought to arise through aberrant mesenchymal stem cell ...
DOI
Add to ORKG