Article
[Clinical applications of molecular diagnosis of retinoblastoma ain 15 families].
Klinische Monatsblatter fur Augenheilkunde - 1 May 1995
Lendi B, Pescia G, Thonney F, Balmer A, Munier F
Abstract excerpt
PURPOSE: In 40% retinoblastoma (Rb) results from a hereditary mutation of the Rb susceptibility gene (RB1). In this study, we tested the usefulness of intragenic DNA analysis for ophthalmologic follow-up in affected families. METHODS: Molecular analysis was performed on 103 DNA samples of 15 Rb f...
Topics
- Adult
- Alleles
- Child
- DNA Mutational Analysis
- Eye Neoplasms
- Female
- Genetic Carrier Screening
- Genetic Counseling
- Humans
- Infant
- Male
- Pedigree
- Polymorphism, Restriction Fragment Length
- Retinoblastoma
- Risk Factors
