Germline intronic and exonic mutations in the Wilms' tumour gene (WT1) affecting urogenital development

This publication has 29 references indexed in Scilit:

• Germline mutations in the Wilms' tumor suppressor gene are associated with abnormal urogenital development in Denys-Drash syndrome
  Cell, 1991
• Exon mutations uncouple 5′ splice site selection from U1 snRNA pairing
  Cell, 1990
• Isolation and characterization of a zinc finger polypeptide gene at the human chromosome 11 Wilms' tumor locus
  Cell, 1990
• Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphisms.
  Proceedings of the National Academy of Sciences, 1989
• A compensatory base change in U1 snRNA suppresses a 5′ splice site mutation
  Cell, 1986
• Mutations in a yeast intron demonstrate the importance of specific conserved nucleotides for the two stages of nuclear mRNA splicing
  Cell, 1986
• A quantitative analysis of the effects of 5′ junction and TACTAAC box mutants and mutant combinations on yeast mRNA splicing
  Cell, 1985
• A point mutation in the conserved hexanucleotide at a yeast 5′ splice junction uncouples recognition, cleavage, and ligation
  Cell, 1985
• An adenovirus mutant defective in splicing RNA from early region 1A
  Nature, 1981
• A syndrome of pseudohermaphroditism, Wilms' tumor, hypertension, and degenerative renal disease
  The Journal of Pediatrics, 1970