Inclusion of new microsatellite repeats in allelic loss analysis excludes retention of heterozygosity in the renal cell carcinoma critical region in 3p21.
- 1 January 2000
- journal article
- Published by Elsevier in Cancer Genetics and Cytogenetics
- Vol. 116 (1) , 40-43
- https://doi.org/10.1016/s0165-4608(99)00094-1
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- A comparison of genomic structures and expression patterns of two closely related flanking genes in a critical lung cancer region at 3p21.3European Journal of Human Genetics, 1999
- Clear-Cell and Papillary Carcinoma of the KidneyCancer Genetics and Cytogenetics, 1998
- Computerized polymorphic marker identification: Experimental validation and a predicted human polymorphism catalogProceedings of the National Academy of Sciences, 1998
- Analysis of multiple renal cell adenomas and carcinomas suggests allelic loss at 3p21 to be a prerequisite for malignant developmentGenes, Chromosomes and Cancer, 1997
- Involvement of multiple loci on chromosome 3 in renal cell cancer developmentGenes, Chromosomes and Cancer, 1997
- Major role for a 3p21 region and lack of involvement of the t(3;8) breakpoint region in the development of renal cell carcinoma suggested by loss of heterozygosity analysisGenes, Chromosomes and Cancer, 1996
- Definition of a tumor suppressor locus within human chromosome 3p21-p22.Proceedings of the National Academy of Sciences, 1992
- Histopathology and Classification of Renal Cell Tumors (Adenomas, Oncocytomas and Carcinomas)Pathology - Research and Practice, 1986