Denys-Drash syndrome: Relating a clinical disorder to genetic alterations in the tumor suppressor gene WT1

This publication has 22 references indexed in Scilit:

• A novel insertional mutation at the third zinc finger coding region of the WT1 gene in Denys— Drash syndrome
  Human Molecular Genetics, 1993
• Constitutional mutations in the WT1 gene in patients with Denys-Drash syndrome
  Human Molecular Genetics, 1992
• Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development
  Nature Genetics, 1992
• Androgen Resistance — The Clinical and Molecular Spectrum
  New England Journal of Medicine, 1992
• Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
  Cell, 1991
• Wilms Tumor Locus on 11p13 Defined by Multiple CpG Island-Associated Transcripts
  Science, 1990
• Clinicopathologic review of twelve children with nephropathy, Wilms tumor, and genital abnormalities (Drash syndrome)
  The Journal of Pediatrics, 1990
• Pseudohermaphroditism, glomerulopathy, and Wilms tumor (Drash syndrome)
  The Journal of Pediatrics, 1985
• Pseudohermaphroditism, glomerulopathy, and Wilms tumor (Drash syndrome): Frequency in end-stage renal failure
  The Journal of Pediatrics, 1985
• A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease
  The Journal of Pediatrics, 1970