Overview of rb gene mutations in patients with retinoblastoma
- 1 August 1998
- journal article
- research article
- Published by Elsevier in Ophthalmology
- Vol. 105 (8) , 1442-1447
- https://doi.org/10.1016/s0161-6420(98)98025-3
Abstract
No abstract availableKeywords
This publication has 27 references indexed in Scilit:
- The Polymerase Chain Reaction (PCR) in the routine genetic characterization of retinoblastoma: A tool for the clinical laboratorySurvey of Ophthalmology, 1997
- Unilateral retinoblastoma: new intraocular tumours after treatment.British Journal of Ophthalmology, 1994
- Mortality From Second Tumors Among Long-Term Survivors of RetinoblastomaJNCI Journal of the National Cancer Institute, 1993
- Regions of the retinoblastoma gene product required for its interaction with the E2F transcription factor are necessary for E2 promoter repression and pRb-mediated growth suppression.Molecular and Cellular Biology, 1993
- Molecular Genetic Diagnosis of RetinoblastomaSeminars in Ophthalmology, 1993
- Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype.Proceedings of the National Academy of Sciences, 1992
- Characterization of deletions at the retinoblastoma locus in patients with bilateral retinoblastomaAmerican Journal of Medical Genetics, 1991
- A single amino acid substitution results in a retinoblastoma protein defective in phosphorylation and oncoprotein binding.Proceedings of the National Academy of Sciences, 1990
- Predicting the risk of hereditary retinoblastoma1American Journal of Ophthalmology, 1988
- The electroencephalogram (EEG) as a research tool in human behavior genetics: Psychological examinations in healthy males with various inherited EEG variantsHuman Genetics, 1979