Polymerase Chain Reaction–Based Risk Assessment for Wilms Tumor in Sporadic Aniridia

This publication has 23 references indexed in Scilit:

• Three novel aniridia mutations in the human PAX6 gene
  Human Mutation, 1995
• Nonsense mutation in the homeobox region of the aniridia gene
  Human Mutation, 1994
• Mutations in the PAX6 gene in patients with hereditary aniridia
  Human Molecular Genetics, 1993
• PAX6 mutations in aniridia
  Human Molecular Genetics, 1993
• Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene
  Nature Genetics, 1992
• The human PAX6 gene is mutated in two patients with aniridia
  Nature Genetics, 1992
• Positional cloning and characterization of a paired box- and homeobox-containing gene from the aniridia region
  Cell, 1991
• Autosomal dominant aniridia linked to the chromosome 11p13 markers catalase and D11S151 in a large Dutch family
  Cytogenetic and Genome Research, 1989
• Aniridia. A review
  Survey of Ophthalmology, 1984
• Aniridia Caused by a Heritable Chromosome 11 Deletion
  Ophthalmology, 1979