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Page 1
Low frequency of hMSH2 mutations in Swedish HNPCC families.
Wahlberg SS, Nyström-Lahti M, Kane MF, Kolodner RD, Peltomäki P, Lindblom A. Wahlberg SS, et al. Among authors: lindblom a. Int J Cancer. 1997 Feb 20;74(1):134-7. doi: 10.1002/(sici)1097-0215(19970220)74:1<134::aid-ijc22>3.0.co;2-e. Int J Cancer. 1997. PMID: 9036882 No abstract available.
A human compound heterozygote for two MLH1 missense mutations.
Hackman P, Tannergård P, Osei-Mensa S, Chen J, Kane MF, Kolodner R, Lambert B, Hellgren D, Lindblom A. Hackman P, et al. Among authors: lindblom a. Nat Genet. 1997 Oct;17(2):135-6. doi: 10.1038/ng1097-135. Nat Genet. 1997. PMID: 9326924 No abstract available.
Ki-ras mutations and prognosis in colorectal cancer.
Kressner U, Bjørheim J, Westring S, Wahlberg SS, Påhlman L, Glimelius B, Lindmark G, Lindblom A, Børresen-Dale AL. Kressner U, et al. Among authors: lindblom a. Eur J Cancer. 1998 Mar;34(4):518-21. doi: 10.1016/s0959-8049(97)10111-3. Eur J Cancer. 1998. PMID: 9713302
Mutation analyses of KRAS exon 1 comparing three different techniques: temporal temperature gradient electrophoresis, constant denaturant capillary electrophoresis and allele specific polymerase chain reaction.
Bjørheim J, Lystad S, Lindblom A, Kressner U, Westring S, Wahlberg S, Lindmark G, Gaudernack G, Ekstrøm P, Røe J, Thilly WG, Børresen-Dale AL. Bjørheim J, et al. Among authors: lindblom a. Mutat Res. 1998 Jul 17;403(1-2):103-12. doi: 10.1016/s0027-5107(98)00057-8. Mutat Res. 1998. PMID: 9726011
517 results