Involvement of 3p Deletions in Sporadic and Hereditary Forms of Renal Cell Carcinoma
- 1 September 1991
- journal article
- Published by Wiley in Genes, Chromosomes and Cancer
- Vol. 3 (5) , 403-406
- https://doi.org/10.1002/gcc.2870030513
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- A genetic model for colorectal tumorigenesisCell, 1990
- A guide to fragile sites on human chromosomesCancer Genetics and Cytogenetics, 1990
- Long-range restriction enzyme maps of DNF15S2, D3S2, and c-raf1 loci on the short arm of human chromosome 3Cancer Genetics and Cytogenetics, 1989
- Report of the committee on the genetic constitution of chromosome 3Cytogenetic and Genome Research, 1989
- Do human renal cell carcinomas arise by a double-loss mechanism?Cancer Genetics and Cytogenetics, 1988
- Translocation t(3;8)(p14.2;q24.1) in renal cell carcinoma affects expression of the common fragile site at 3p14(FRA3B) in lymphocytesCancer Genetics and Cytogenetics, 1988
- Consistent chromosome 3p deletion and loss of heterozygosity in renal cell carcinoma.Proceedings of the National Academy of Sciences, 1988
- Chromosome localization of the human oncogene INTl to 12ql3 by in situ hybridizationCytogenetic and Genome Research, 1988
- Deletion of a DNA sequence at the chromosomal region 3p21 in all major types of lung cancerNature, 1987
- Hereditary Renal-Cell Carcinoma Associated with a Chromosomal TranslocationNew England Journal of Medicine, 1979