Nephroblastoma or Wilms\u27 tumor is a pediatric renal malignancy that is the most frequently occurring childhood solid tumor. Approximately 1-2% of children with Wilms\u27 tumor also present with aniridia, a congenital absence of all or part of the iris of the eye. These children also have high rates of genitourinary anomalies and mental retardation resulting in what is called the WAGR (Wilms\u27 tumor, aniridia, genitourinary anomaly, mental retardation) syndrome. Cytogenetic analysis of metaphase chromosomes from these patients revealed a consistent deletion of band P13 on chromosome 11. These observations suggest close physical linkage between the disease-related loci, and further imply that development of each phenotype results from th...
Wilms' tumor is a childhood nephroblastoma that is postulated to arise through the inactivation of a...
A long-range restriction map of part of the short arm of ehromosome 11 including the WAGR region has...
A series of 125 patients referred primarily with aniridia classified as either sporadic (74), famili...
Nephroblastoma or Wilms\u27 tumor is a pediatric renal malignancy that is the most frequently occurr...
The WAGR (Wilms tumor, aniridia, genitourinary anomalies, and mental retardation) region has been as...
Chromosome 11p13 is frequently rearranged in individuals with the WAGR syndrome (Wilms tumor, anirid...
Fusion of an auxotrophic mutant hamster cell with the skin fibroblasts of a child with the Wilms' tu...
Wilms\u27 tumor (WT) is a childhood embryonic tumor of the kidney. In some cases, WT has been associ...
Seventy-seven patients with aniridia, referred for cytogenetic analysis predominantly to assess Wilm...
Seventy-seven patients with aniridia, referred for cytogenetic analysis predominantly to assess Wilm...
Conventional cytogenetic studies on a female infant with sporadic aniridia revealed what appeared to...
To understand genetic and epigenetic pathways in Wilms ’ tumors, we carried out a genome scan for lo...
Chromosome 11p15 has been suggested to be a potential site for a second Wilms' tumour gene (a childh...
Wilms' tumour is an embryonic kidney tumour thought to arise through aberrant mesenchymal stem cell ...
Cytogenetic analysis of predisposition syndromes has played a critical role in the elucidation of th...
Wilms' tumor is a childhood nephroblastoma that is postulated to arise through the inactivation of a...
A long-range restriction map of part of the short arm of ehromosome 11 including the WAGR region has...
A series of 125 patients referred primarily with aniridia classified as either sporadic (74), famili...
Nephroblastoma or Wilms\u27 tumor is a pediatric renal malignancy that is the most frequently occurr...
The WAGR (Wilms tumor, aniridia, genitourinary anomalies, and mental retardation) region has been as...
Chromosome 11p13 is frequently rearranged in individuals with the WAGR syndrome (Wilms tumor, anirid...
Fusion of an auxotrophic mutant hamster cell with the skin fibroblasts of a child with the Wilms' tu...
Wilms\u27 tumor (WT) is a childhood embryonic tumor of the kidney. In some cases, WT has been associ...
Seventy-seven patients with aniridia, referred for cytogenetic analysis predominantly to assess Wilm...
Seventy-seven patients with aniridia, referred for cytogenetic analysis predominantly to assess Wilm...
Conventional cytogenetic studies on a female infant with sporadic aniridia revealed what appeared to...
To understand genetic and epigenetic pathways in Wilms ’ tumors, we carried out a genome scan for lo...
Chromosome 11p15 has been suggested to be a potential site for a second Wilms' tumour gene (a childh...
Wilms' tumour is an embryonic kidney tumour thought to arise through aberrant mesenchymal stem cell ...
Cytogenetic analysis of predisposition syndromes has played a critical role in the elucidation of th...
Wilms' tumor is a childhood nephroblastoma that is postulated to arise through the inactivation of a...
A long-range restriction map of part of the short arm of ehromosome 11 including the WAGR region has...
A series of 125 patients referred primarily with aniridia classified as either sporadic (74), famili...