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Results:
1-7
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Results: 7
Authors:
Finnila, S
Majamaa, K
Citation: S. Finnila et K. Majamaa, Phylogenetic analysis of mtDNA haplogroup TJ in a Finnish population, J HUM GENET, 46(2), 2001, pp. 64-69
Authors:
Finnila, S
Tuisku, S
Herva, R
Majamaa, K
Citation: S. Finnila et al., A novel mitochondrial DNA mutation and a mutation in the Notch3 gene in a patient with myopathy and CADASIL, J MOL MED-J, 79(11), 2001, pp. 641-647
Authors:
Finnila, S
Autere, J
Lehtovirta, M
Hartikainen, P
Mannermaa, A
Soininen, H
Majamaa, K
Citation: S. Finnila et al., Increased risk of sensorineural hearing loss and migraine in patients witha rare mitochondrial DNA variant 4336A > G in tRNA(Gln), J MED GENET, 38(6), 2001, pp. 400-405
Authors:
Finnila, S
Lehtonen, MS
Majamaa, K
Citation: S. Finnila et al., Phylogenetic network for European mtDNA, AM J HU GEN, 68(6), 2001, pp. 1475-1484
Authors:
Meinila, M
Finnila, S
Majamaa, K
Citation: M. Meinila et al., Evidence for mtDNA admixture between the Finns and the Saami, HUMAN HERED, 52(3), 2001, pp. 160-170
Authors:
Finnila, S
Hassinen, IE
Ala-Kokko, L
Majamaa, K
Citation: S. Finnila et al., Phylogenetic network of the mtDNA haplogroup U in northern Finland based on sequence analysis of the complete coding region by conformation-sensitivegel electrophoresis, AM J HU GEN, 66(3), 2000, pp. 1017-1026
Authors:
Sajanti, J
Bjorkstrand, AS
Finnila, S
Heikkinen, E
Peltonen, J
Majamaa, K
Citation: J. Sajanti et al., Increase of collagen synthesis and deposition in the arachnoid and the dura following subarachnoid hemorrhage in the rat, BBA-MOL BAS, 1454(3), 1999, pp. 209-216
Risultati:
1-7
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