Search
WT1 gene mutation
Clinical manifestations: - defects in WT1 are the cause of a) Frasier syndrome b) genitourinary dysplasia component of WAGR syndrome c) Wilms tumor 1 d) Denys-Drash syndrome e) isolated diffuse mesangial sclerosis f) Meacham syndrome g) hypospadiasRelated
Wilms' tumor protein; WT1 protein (WT1, WT3) WT1 mRNA expression in blood/tissueGeneral
gene mutation testing; gene mutation analysisReferences
- Loinc