Detection of chromosome imbalances in retinoblastoma by parallel karyotype and CGH analyses
- 14 June 2000
- journal article
- research article
- Published by Wiley in Genes, Chromosomes and Cancer
- Vol. 28 (4) , 370-379
- https://doi.org/10.1002/1098-2264(200008)28:4<370::aid-gcc2>3.0.co;2-8
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- Molecular characterization of a novel amplicon at 1q21-q22 frequently observed in human sarcomas.British Journal of Cancer, 1998
- Polymerase chain reaction compared with dot blotting for the determination of N-myc gene amplification in neuroblastomaInternational Journal of Cancer, 1997
- N-MYC amplification, loss of heterozygosity on the short arm of chromosome 1 and DNA ploidy in retinoblastomaEuropean Journal Of Cancer, 1996
- Phenotype variants, malignancy, and additional copies of 6p in retinoblastomaCancer Genetics and Cytogenetics, 1994
- Amplification of a DEAD box protein gene in retinoblastoma cell lines.Proceedings of the National Academy of Sciences, 1993
- Genetics and cytogenetics of retinoblastomaCancer Genetics and Cytogenetics, 1992
- Amplification of the human putative oncogene INT1 in primary retinoblastoma tumorsCytogenetic and Genome Research, 1988
- Re-evaluation of the sublocalization of esterase D and its relation to the retinoblastoma locus by in situ hybridizationCytogenetic and Genome Research, 1987
- Cytogenetic analysis of retinoblastoma: evidence for multifocal origin and in vivo gene amplificationCytogenetic and Genome Research, 1984
- Expression of recessive alleles by chromosomal mechanisms in retinoblastomaNature, 1983