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Results:
1-16
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Results: 16
Authors:
Raitio, M
Lindroos, K
Laukkanen, M
Pastinen, T
Sistonen, P
Sajantila, A
Syvanen, AC
Citation: M. Raitio et al., Y-chromosomal SNPs in Finno-Ugric-speaking populations analyzed by minisequencing on microarrays, GENOME RES, 11(3), 2001, pp. 471-482
Authors:
Daniels, GL
Anstee, DJ
Cartron, JP
Dahr, W
Fletcher, A
Garratty, G
Henry, S
Jorgensen, J
Judd, WJ
Kornstad, L
Levene, C
Lin, M
Lomas-Francis, C
Lubenko, A
Moulds, JJ
Moulds, JM
Moulds, M
Overbeeke, M
Reid, ME
Rouger, P
Scott, M
Sistonen, P
Smart, E
Tani, Y
Wendel, S
Zelinski, T
Citation: Gl. Daniels et al., International Society of Blood Transfusion working party on terminology for red cell surface antigens, VOX SANGUIN, 80(3), 2001, pp. 193-196
Authors:
Launonen, V
Vierimaa, O
Kiuru, M
Isola, J
Roth, S
Pukkala, E
Sistonen, P
Herva, R
Aaltonen, LA
Citation: V. Launonen et al., Inherited susceptibility to uterine leiomyomas and venal cell cancer, P NAS US, 98(6), 2001, pp. 3387-3392
Authors:
Kiuru, M
Launonen, V
Hietala, M
Aittomaki, K
Vierimaa, O
Salovaara, R
Arola, J
Pukkala, E
Sistonen, P
Herva, R
Aaltonen, LA
Citation: M. Kiuru et al., Familial cutaneous leiomyomatosis is a two-hit condition associated with renal cell cancer of characteristic histopathology, AM J PATH, 159(3), 2001, pp. 825-829
Authors:
Lund, A
Udd, B
Juvonen, V
Andersen, PM
Cederquist, K
Ronnevi, LO
Sistonen, P
Sorensen, SA
Tranebjaerg, L
Wallgren-Pettersson, C
Savontaus, ML
Citation: A. Lund et al., Founder effect in spinal and bulbar muscular atrophy (SBMA) in Scandinavia, EUR J HUM G, 8(8), 2000, pp. 631-636
Authors:
Jonasson, J
Juvonen, V
Sistonen, P
Ignatius, J
Johansson, D
Bjorck, EJ
Wahlstrom, J
Melberg, A
Holmgren, G
Forsgren, L
Holmberg, M
Citation: J. Jonasson et al., Evidence for a common Spinocerebellar ataxia type 7 (SCA7) founder mutation in Scandinavia, EUR J HUM G, 8(12), 2000, pp. 918-922
Authors:
Lahermo, P
Laitinen, V
Sistonen, P
Beres, J
Karcagi, V
Savontaus, ML
Citation: P. Lahermo et al., MtDNA polymorphism in the Hungarians: comparison to three other Finno-Ugric-speaking populations, HEREDITAS, 132(1), 2000, pp. 35-42
Authors:
Sidoux-Walter, F
Lucien, N
Nissinen, R
Sistonen, P
Henry, S
Moulds, J
Cartron, JP
Bailly, P
Citation: F. Sidoux-walter et al., Molecular heterogeneity of the Jk(null) phenotype: expression analysis of the Jk(S291P) mutation found in Finns, BLOOD, 96(4), 2000, pp. 1566-1573
Authors:
Roth, S
Sistonen, P
Salovaara, R
Hemminki, A
Loukola, A
Johansson, M
Avizienyte, E
Cleary, KA
Lynch, P
Amos, CI
Kristo, P
Mecklin, JP
Kellokumpu, I
Jarvinen, H
Aaltonen, LA
Citation: S. Roth et al., SMAD genes in juvenile polyposis, GENE CHROM, 26(1), 1999, pp. 54-61
Authors:
Lahermo, P
Savontaus, ML
Sistonen, P
Beres, J
de Knijff, P
Aula, P
Sajantila, A
Citation: P. Lahermo et al., Y chromosomal polymorphisms reveal founding lineages in the Finns and the Saami, EUR J HUM G, 7(4), 1999, pp. 447-458
Authors:
Levo, A
Jaaskelainen, J
Sistonen, P
Siren, MK
Voutilainen, R
Partanen, J
Citation: A. Levo et al., Tracing past population migrations: genealogy of steroid 21-hydroxylase (CYP21) gene mutations in Finland, EUR J HUM G, 7(2), 1999, pp. 188-196
Authors:
Ylikorkala, A
Avizienyte, E
Tomlinson, IPM
Tiainen, M
Roth, S
Loukola, A
Hemminki, A
Johansson, M
Sistonen, P
Markie, D
Neale, K
Phillips, R
Zauber, P
Twama, T
Sampson, J
Jarvinen, H
Makela, TP
Aaltonen, LA
Citation: A. Ylikorkala et al., Mutations and impaired function of LKB1 in familial and non-familial Peutz-Jeghers syndrome and a sporadic testicular cancer, HUM MOL GEN, 8(1), 1999, pp. 45-51
Authors:
Daniels, GL
Anstee, DJ
Cartron, JP
Dahr, W
Garratty, G
Henry, S
Jorgensen, J
Judd, WJ
Kornstad, L
Levene, C
Lomas-Francis, C
Lubenko, A
Moulds, JJ
Moulds, JM
Moulds, M
Overbeeke, M
Reid, ME
Rouger, P
Scott, M
Seidl, S
Sistonen, P
Tani, Y
Wendel, S
Zelinski, T
Citation: Gl. Daniels et al., Terminology for red cell surface antigens - ISBT Working Party Oslo Report, VOX SANGUIN, 77(1), 1999, pp. 52-57
Authors:
Sistonen, P
Virtaranta-Knowles, K
Denisova, R
Kucinskas, V
Ambrasiene, D
Beckman, L
Citation: P. Sistonen et al., The LWb blood group as a marker of prehistoric Baltic migrations and admixture, HUMAN HERED, 49(3), 1999, pp. 154-158
Authors:
Holopainen, P
Arvas, M
Sistonen, P
Mustalahti, K
Collin, P
Maki, M
Partanen, J
Citation: P. Holopainen et al., CD28/CTLA4 gene region on chromosome 2q33 confers genetic susceptibility to celiac disease. A linkage and family-based association study, TISSUE ANTI, 53(5), 1999, pp. 470-475
Authors:
Moisio, AL
Sistonen, P
Mecklin, JP
Jarvinen, H
Peltomaki, P
Citation: Al. Moisio et al., Genetic polymorphisms in carcinogen metabolism and their association to hereditary nonpolyposis colon cancer, GASTROENTY, 115(6), 1998, pp. 1387-1394
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1-16
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