- Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations2010 | 2. lékařská fakulta
- Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 92006 | 2. lékařská fakulta
- Clinical relevance of Wilms tumor 1 gene mutations in childhood acute myeloid leukemia2009 | 2. lékařská fakulta
- No Prognostic Impact of the WT1 Gene Single Nucleotide Polymorphism rs16754 in Pediatric Acute Myeloid Leukemia2010 | 2. lékařská fakulta
- Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome2012 | 2. lékařská fakulta
- Standardization of WT1 mRNA quantitation for minimal residual disease monitoring in childhood AML and implications of WT1 gene mutations: a European multicenter study2009 | 2. lékařská fakulta
- The clinical relevance of BAALC and ERG expression levels in pediatric AML2013 | 2. lékařská fakulta
- NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression pattern2011 | 2. lékařská fakulta
- Genotype-phenotype associations in WT1 glomerulopathy2014 | 2. lékařská fakulta
- Souhrnná analýza aberací prvního a druhého typu zkresluje genetickou heterogenitu dětské akutní myeloidní leukémie2011 | 1. lékařská fakulta
- Integrative analysis of type-I and type-II aberrations underscores the genetic heterogeneity of pediatric acute myeloid leukemia2011 | 2. lékařská fakulta