Molecular insight into multiple Wilms tumors arising in germline WT1-mutated/11p13-deleted patients

Pediatr Blood Cancer. 2018 Nov;65(11):e27360. doi: 10.1002/pbc.27360. Epub 2018 Jul 17.

Author

Daniela Perotti¹

Affiliation

¹ Molecular Bases of Genetic Risk and Genetic Testing Unit, Department of Research, Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy.

PMID: 30015390
DOI: 10.1002/pbc.27360

No abstract available

Publication types

Comment

MeSH terms

Genes, Wilms Tumor
Germ Cells
Humans
Kidney Neoplasms / genetics*
Loss of Heterozygosity
WT1 Proteins
Wilms Tumor / genetics*

Substances

WT1 Proteins
WT1 protein, human