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Finnish mutations in Swedish HNPCC families.
Tannergård P, Nordenskjöld M, Lindblom A. Tannergård P, et al. Among authors: lindblom a. Nat Med. 1995 Nov;1(11):1104. doi: 10.1038/nm1195-1104b. Nat Med. 1995. PMID: 7584969 No abstract available.
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 Free article. No abstract available.
Molecular basis of HNPCC: mutations of MMR genes.
Papadopoulos N, Lindblom A. Papadopoulos N, et al. Among authors: lindblom a. Hum Mutat. 1997;10(2):89-99. doi: 10.1002/(SICI)1098-1004(1997)10:2<89::AID-HUMU1>3.0.CO;2-H. Hum Mutat. 1997. PMID: 9259192 Review.
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.
505 results