The genetics of retinoblastoma

This publication has 44 references indexed in Scilit:

• PRENATAL EXCLUSION OF HEREDITARY RETINOBLASTOMA
  The Lancet, 1988
• Prediction of the Risk of Hereditary Retinoblastoma, Using DNA Polymorphisms within the Retinoblastoma Gene
  New England Journal of Medicine, 1988
• Deletions of a DNA sequence in retinoblastomas and mesenchymal tumors: organization of the sequence and its encoded protein.
  Proceedings of the National Academy of Sciences, 1987
• Deletion (13) (q14.1q14.3) in two generations: Variability of ocular manifestations and definition of the phenotype
  American Journal of Medical Genetics, 1987
• The retinoblastoma susceptibility gene encodes a nuclear phosphoprotein associated with DNA binding activity
  Nature, 1987
• Structural Evidence for the Authenticity of the Human Retinoblastoma Gene
  Science, 1987
• An assessment of the usefulness of electrophoretic variants of esterase-D in the antenatal diagnosis of retinoblastoma in the United Kingdom
  British Journal of Cancer, 1987
• Human Retinoblastoma Susceptibility Gene: Cloning, Identification, and Sequence
  Science, 1987
• Molecular detection of deletions involving band q14 of chromosome 13 in retinoblastomas.
  Proceedings of the National Academy of Sciences, 1986
• Chromosome deletion in a case of retinoblastoma
  Annals of Human Genetics, 1963