1. deletions in human colorectal carcinomas: cytogenetics and restiction fragment length polymorphism analysis;Keldysh, P.L.; Dragani, T.A.; Fleischman, E.W.; Konstaninova, L.N.; Perevoschiskov, A.G.; Pierotti, M.A.;Genes Chronzosom Cancer,1993
2. Loss of heterozygosity and amplification on chromosome 11 q in human ovarian cancer;Foulkes, W.D.; Campbell, I.G.; Stamp, J.W.; Trowsdale, J.;BrJI Cancer,1993
3. Loss of heterozygosity in malignant melanoma at loci on chromosomes 11 and 17 implicated in the pathogenesis of other cancers. Genes Chromosom;Tomlinson, I.P.M.; Gammack, A.J.; Stickland, J.E.; Mann, G.J.; Mackie, R.M.; Kefford, R.F.;Cancer,1993
4. Identification and chromosomal localisation of a DNA fragment implicated in the partial correction of the Fanconi amaemia group D cellular defect;Diatloff-Zito, C.; Duchaud, E.; Viegas-Pequignot, E.; Fraser, D.; Moustacchi, E.;Mutation Res,1994
5. Refinement of regional loss of heterozygosity for chromosome l 1p 1.5 in human breast tumours;Winquist, R.; Mannermaa, A.; Alavaikko, M.; Blanco, G.; Taskine, P.J.; Kiviniemi, H.;Cancer Res,1993