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Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked disease.
Suomalainen A, Majander A, Wallin M, Setälä K, Kontula K, Leinonen H, Salmi T, Paetau A, Haltia M, Valanne L, Lonnqvist J, Peltonen L, Somer H. Suomalainen A, et al. Among authors: lonnqvist j. Neurology. 1997 May;48(5):1244-53. doi: 10.1212/wnl.48.5.1244. Neurology. 1997. PMID: 9153451
Schizophrenia in the genetic isolate of Finland.
Hovatta I, Terwilliger JD, Lichtermann D, Mäkikyrö T, Suvisaari J, Peltonen L, Lönnqvist J. Hovatta I, et al. Among authors: lonnqvist j. Am J Med Genet. 1997 Jul 25;74(4):353-60. Am J Med Genet. 1997. PMID: 9259368
Assignment of the locus for PLO-SL, a frontal-lobe dementia with bone cysts, to 19q13.
Pekkarinen P, Hovatta I, Hakola P, Järvi O, Kestilä M, Lenkkeri U, Adolfsson R, Holmgren G, Nylander PO, Tranebjaerg L, Terwilliger JD, Lönnqvist J, Peltonen L. Pekkarinen P, et al. Among authors: lonnqvist j. Am J Hum Genet. 1998 Feb;62(2):362-72. doi: 10.1086/301722. Am J Hum Genet. 1998. PMID: 9463329 Free PMC article.
Attitudes towards genetic testing: analysis of contradictions.
Jallinoja P, Hakonen A, Aro AR, Niemelä P, Hietala M, Lönnqvist J, Peltonen L, Aula P. Jallinoja P, et al. Among authors: lonnqvist j. Soc Sci Med. 1998 May;46(10):1367-74. doi: 10.1016/s0277-9536(98)00017-3. Soc Sci Med. 1998. PMID: 9665567
592 results