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Last Updated: 01/07/2026
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Found 149 publications
A novel variant leads to WT1-related nephrotic syndrome and differences of sex development: a case report.
Journal: Frontiers in pediatrics
Published: July 01, 2025
WT1-Related Nephropathy in a Phenotypically Female Child: A Case of Clinical and Genetic Discordance.
Journal: Children (Basel, Switzerland)
Published: March 20, 2025
Immunosuppressant-resistant nephrotic syndrome and primary amenorrhea: A case report of adult Frasier syndrome and literature review.
Journal: Clinical nephrology
Published: July 22, 2024
A review of the genetic background in complicated WT1-related disorders.
Journal: Clinical and experimental nephrology
Published: May 07, 2024
Evaluation of pathogenicity of WT1 intron variants by in vitro splicing analysis.
Journal: Clinical and experimental nephrology
Published: December 07, 2023
Wilms' tumor gene 1: lessons from the interface between kidney development and cancer.
Journal: American journal of physiology. Renal physiology
Published: November 02, 2023
The -KTS splice variant of WT1 is essential for ovarian determination in mice.
Journal: Science (New York, N.Y.)
Published: November 02, 2023
WT1-related disorders: more than Denys-Drash syndrome.
Journal: Pediatric nephrology (Berlin, Germany)
Published: October 03, 2023
High-Throughput Splicing Assays Identify Known and Novel WT1 Exon 9 Variants in Nephrotic Syndrome.
Journal: Kidney international reports
Published: June 09, 2023
Genotype-phenotype correlation of WT1 mutation-related nephropathy in Chinese children.
Journal: Frontiers in pediatrics
Published: March 22, 2023
Frasier Syndrome: A 15-Year-Old Phenotypically Female Adolescent Presenting with Delayed Puberty and Nephropathy.
Journal: Children (Basel, Switzerland)
Published: February 02, 2023
Last Updated: 01/07/2026