Related Experiment Videos
Parental origin of WT1 mutations and mental retardation in WAGR syndrome
Nature Genetics
|September 1, 1994
Abstract
No abstract available in PubMed .
Related Concept Videos
Articles linked to this work by shared authors, journal, and citation graph.
Treatment with nephrectomy only for small, stage I/favorable histology Wilms' tumor: a report from the National Wilms' Tumor Study Group.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology·2001
Absence of PPP2R1A mutations in Wilms tumor.
Oncogene·2001
Pulmonary dysplasia, Denys-Drash syndrome and Wilms tumor 1 gene mutation in twins.
Pediatric nephrology (Berlin, Germany)·2001
Frequent association of beta-catenin and WT1 mutations in Wilms tumors.
Cancer research·2000
Familial Wilms' tumor with neural elements: characterization by histology, immunohistochemistry, and genetic analysis.
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society·2000
Mutation in the PAX6 gene in twenty patients with aniridia.
Human mutation·2000
Establishing Polycomb regulatory landscapes in human early development.
Nature genetics·2026
Single-allele nanoscale mapping of regulatory variants.
Nature genetics·2026
Familial factors in SARS-CoV-2 susceptibility and COVID-19 severity: a nationwide Danish study of adult twins and their spouses.
International journal of epidemiology·2026
The monogenic forms of obesity in Saudi families.
Human molecular genetics·2026
Screening for beta thalassemia trait in a heterogeneous university-based population in Delhi-NCR, India.
Journal of community genetics·2026
Genome-wide characterisation of leaf rust resistance loci in an Eastern European barley collection.
TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik·2026