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wt1 mutations
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Genotype/Phenotype Correlation in Nephrotic Syndrome Caused by WT1 Mutations
2010 |
Second Faculty of Medicine
publication
Mutations in the Wilms' tumor 1 gene cause isolated steroid resistant nephrotic syndrome and occur in exons 8 and 9
2006 |
Second Faculty of Medicine
publication
Clinical relevance of Wilms tumor 1 gene mutations in childhood acute myeloid leukemia
2009 |
Second Faculty of Medicine
publication
No Prognostic Impact of the WT1 Gene Single Nucleotide Polymorphism rs16754 in Pediatric Acute Myeloid Leukemia
2010 |
Second Faculty of Medicine
publication
Discordant expression of a new WT1 gene mutation in a family with monozygotic twins presenting with congenital nephrotic syndrome
2012 |
Second Faculty of Medicine
publication
Standardization of WT1 mRNA quantitation for minimal residual disease monitoring in childhood AML and implications of WT1 gene mutations: a European multicenter study
2009 |
Second Faculty of Medicine
publication
The clinical relevance of BAALC and ERG expression levels in pediatric AML
2013 |
Second Faculty of Medicine
publication
NUP98/NSD1 characterizes a novel poor prognostic group in acute myeloid leukemia with a distinct HOX gene expression pattern
2011 |
Second Faculty of Medicine
publication
Genotype-phenotype associations in WT1 glomerulopathy
2014 |
Second Faculty of Medicine
publication
Integrative analysis of type-I and type-II aberrations underscores the genetic heterogeneity of pediatric acute myeloid leukemia
2011 |
First Faculty of Medicine
publication
Integrative analysis of type-I and type-II aberrations underscores the genetic heterogeneity of pediatric acute myeloid leukemia
2011 |
Second Faculty of Medicine