Minimal regions of chromosomal imbalance in retinoblastoma detected by comparative genomic hybridization
- 1 August 2001
- journal article
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 129 (1) , 57-63
- https://doi.org/10.1016/s0165-4608(01)00427-7
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Detection of chromosome imbalances in retinoblastoma by parallel karyotype and CGH analysesGenes, Chromosomes and Cancer, 2000
- Optimizing comparative genomic hybridization for analysis of DNA sequence copy number changes in solid tumorsGenes, Chromosomes and Cancer, 1994
- Comparative Genomic Hybridization for Molecular Cytogenetic Analysis of Solid TumorsScience, 1992
- Mice deficient for Rb are nonviable and show defects in neurogenesis and haematopoiesisNature, 1992
- A detailed analysis of chromosomal changes in heritable and non-heritable retinoblastomaHuman Genetics, 1985
- Genetic Origin of Mutations Predisposing to RetinoblastomaScience, 1985
- Isochromosome 6p, a unique chromosomal abnormality in retinoblastoma: Verification by standard staining techniques, new densitometric methods, and somatic cell hybridizationHuman Genetics, 1984
- Somatic inactivation of genes on chromosome 13 is a common event in retinoblastomaNature, 1983
- Similar chromosomal abnormalities in several retinoblastomasHuman Genetics, 1982
- Mutation and Cancer: Statistical Study of RetinoblastomaProceedings of the National Academy of Sciences, 1971