Condition: WAGR Syndrome


rs121907909 in WT1 gene and WAGR Syndrome PMID 9108089 1997 Correlation of germ-line mutations and two-hit inactivation of the WT1 gene with Wilms tumors of stromal-predominant histology.

PMID 21851196 2011 Clinical pictures and novel mutations of WT1-associated Denys-Drash syndrome in two Chinese children.

PMID 23515051 2013 Genetic screening in adolescents with steroid-resistant nephrotic syndrome.

PMID 10571943 1999 Exon 9 mutations in the WT1 gene, without influencing KTS splice isoforms, are also responsible for Frasier syndrome.

PMID 15150775 2004 Twenty-four new cases of WT1 germline mutations and review of the literature: genotype/phenotype correlations for Wilms tumor development.