Product Description
This text describes the clinical pathological and molecular genetic features that characterize Wilms tumour, the most common renal tumour of infancy. The book notes that the heterogeneity observed at the clinical pathological level is also seen at the molecular genetic level. This suggests that the molecular events leading to Wilms tumour are complex, but at the same time provide a paradigm for other embryonal and adult malignancies.
--This text refers to an out of print or unavailable edition of this title.







