Therese Törngren

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2001
Mark Haplotype analysis and age estimation of the 113insR CDKN2A founder mutation in Swedish melanoma families
Hashemi, Jamileh ; Bendahl, Pär-Ola ^LU ; Törngren, Therese ^LU ; Platz, Anton ; Linder, Stig ; Stierner, Ulrika ; Olsson, Håkan ^LU ; Ingvar, Christian ^LU ; Hansson, Johan and Borg, Åke ^LU (2001) In Genes, Chromosomes and Cancer 31(2). p.107-116
- Contribution to journal › Article
2000
Mark Somatic deletions in hereditary breast cancers implicate 13q21 as a putative novel breast cancer susceptibility locus
Kainu, T ; Juo, S H ; Desper, R ; Schaffer, A A ; Gillanders, E ; Rozenblum, E ; Freas-Lutz, D ; Weaver, D ; Stephan, D and Bailey-Wilson, J , et al. (2000) In Proceedings of the National Academy of Sciences 97(17). p.9603-9608
- Contribution to journal › Article
1999
Mark Isochromosome 17q in blast crisis of chronic myeloid leukemia and in other hematologic malignancies is the result of clustered breakpoints in 17p11 and is not associated with coding TP53 mutations
Fioretos, Thoas ^LU ; Strömbeck, Bodil ^LU ; Törngren, Therese ^LU ; Johansson, Bertil ^LU ; Billstrom, Rolf ; Borg, Åke ^LU ; Nilsson, Per-Gunnar ^LU ; Van Den Berghe, Herman ; Hagemeijer, Anne and Mitelman, Felix ^LU , et al. (1999) In Blood 94(1). p.225-232
- Contribution to journal › Article

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