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Mutation Research|June 1, 1993
Molecular analysis of mutations in the hprt gene in circulating lymphocytes from normal and DNA-repair-deficient donorsH Steingrimsdottir, G Rowley, A Waugh, et al.
British Journal of Cancer|July 1, 1996
Loss of heterozygosity on chromosome 5q in ovarian cancer is frequently accompanied by TP53 mutation and identifies a tumour suppressor gene locus at 5q13.1-21M Tavassoli, H Steingrimsdottir, E Pierce, et al.
Journal of Oral Pathology & Medicine : Official Publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology|April 4, 1998
p53 aberrations in oral submucous fibrosis and oral squamous cell carcinoma detected by immunocytochemistry and PCR-SSCPC Trivedy, K A Warnakulasuriya, M Tavassoli, et al.
Mutation Research|June 12, 1996
Development of new molecular procedures for the detection of genetic alterations in manH Steingrimsdottir, D Beare, J Cole, et al.
British Journal of Cancer|July 2, 1999
Role of p16/MTS1, cyclin D1 and RB in primary oral cancer and oral cancer cell linesM Sartor, H Steingrimsdottir, F Elamin, et al.
Molecular and Cellular Biology|March 1, 1997
Molecular and biochemical characterization of xrs mutants defective in Ku80B K Singleton, A Priestley, H Steingrimsdottir, et al.
American Journal of Human Genetics|March 7, 1998
Molecular analysis of mutations in the CSB (ERCC6) gene in patients with Cockayne syndromeD L Mallery, B Tanganelli, S Colella, et al.
Environmental and Molecular Mutagenesis|January 1, 1997
Correlated mutagenesis of bcl2 and hprt loci in blood lymphocytesY Liu, G Cortopassi, H Steingrimsdottir, et al.
Cancer Research|November 15, 1988
Relation between the human fibroblast strain 46BR and cell lines representative of Bloom's syndromeA R Lehmann, A E Willis, B C Broughton, et al.
Molecular and Cellular Biology|April 1, 1987
Inactivation of a transfected gene in human fibroblasts can occur by deletion, amplification, phenotypic switching, or methylationM M Gebara, C Drevon, S A Harcourt, et al.
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