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Results: 1-15 |
Results: 15
Y-chromosomal SNPs in Finno-Ugric-speaking populations analyzed by minisequencing on microarrays
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
DNA Commission of the International Society of Forensic Genetics: recommendations on forensic analysis using Y-chromosome STRs
Authors: Gill, P Brenner, C Brinkmann, B Budowle, B Carracedo, A Jobling, MA de Knijff, P Kayser, M Krawczak, M Mayr, WR Morling, N Olaisen, B Pascali, V Prinz, M Roewer, L Schneider, PM Sajantila, A Tyler-Smith, C
Citation: P. Gill et al., DNA Commission of the International Society of Forensic Genetics: recommendations on forensic analysis using Y-chromosome STRs, INT J LEGAL, 114(6), 2001, pp. 305-309
Recent insertion of an Alu element within a polymorphic human-specific Aluinsertion
Authors: Comas, D Plaza, S Calafell, F Sajantila, A Bertranpetit, J
Citation: D. Comas et al., Recent insertion of an Alu element within a polymorphic human-specific Aluinsertion, MOL BIOL EV, 18(1), 2001, pp. 85-88
Forensic osteological investigations in Kosovo
Authors: Rainio, J Hedman, M Karkola, K Lalu, K Peltola, P Ranta, H Sajantila, A Soderholm, N Penttila, A
Citation: J. Rainio et al., Forensic osteological investigations in Kosovo, FOREN SCI I, 121(3), 2001, pp. 166-173
Mutations at Y-STR loci: implications for paternity testing and forensic analysis
Authors: Kayser, M Sajantila, A
Citation: M. Kayser et A. Sajantila, Mutations at Y-STR loci: implications for paternity testing and forensic analysis, FOREN SCI I, 118(2-3), 2001, pp. 116-121
Homozygosity for a HERG potassium channel mutation causes a severe form oflong-QT syndrome: Identification of an apparent founder mutation in the Finns
Authors: Piippo, K Laitinen, P Swan, H Toivonen, L Viitasalo, M Pasternack, M Paavonen, K Chapman, H Wann, KT Hirvela, E Sajantila, A Kontula, K
Citation: K. Piippo et al., Homozygosity for a HERG potassium channel mutation causes a severe form oflong-QT syndrome: Identification of an apparent founder mutation in the Finns, J AM COL C, 35(7), 2000, pp. 1919-1925
Alu insertion polymorphisms in NW Africa and the Iberian Peninsula: evidence for a strong genetic boundary through the Gibraltar Straits
Authors: Comas, D Calafell, F Benchemsi, N Helal, A Lefranc, G Stoneking, M Batzer, MA Bertranpetit, J Sajantila, A
Citation: D. Comas et al., Alu insertion polymorphisms in NW Africa and the Iberian Peninsula: evidence for a strong genetic boundary through the Gibraltar Straits, HUM GENET, 107(4), 2000, pp. 312-319
Characteristics and frequency of germline mutations at microsatellite locifrom the human Y chromosome, as revealed by direct observation in father/son pairs
Authors: Kayser, M Roewer, L Hedman, M Henke, L Henke, J Brauer, S Kruger, C Krawczak, M Nagy, M Dobosz, T Szibor, R de Knijff, P Stoneking, M Sajantila, A
Citation: M. Kayser et al., Characteristics and frequency of germline mutations at microsatellite locifrom the human Y chromosome, as revealed by direct observation in father/son pairs, AM J HU GEN, 66(5), 2000, pp. 1580-1588
Evidence for variable selective pressures at MC1R
Authors: Harding, RM Healy, E Ray, AJ Ellis, NS Flanagan, N Todd, C Dixon, C Sajantila, A Jackson, IJ Birch-Machin, MA Rees, JL
Citation: Rm. Harding et al., Evidence for variable selective pressures at MC1R, AM J HU GEN, 66(4), 2000, pp. 1351-1361
Y chromosomal polymorphisms reveal founding lineages in the Finns and the Saami
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
Analysis of mtDNA HVRII in several human populations using an immobilised SSO probe hybridisation assay
Authors: Comas, D Reynolds, R Sajantila, A
Citation: D. Comas et al., Analysis of mtDNA HVRII in several human populations using an immobilised SSO probe hybridisation assay, EUR J HUM G, 7(4), 1999, pp. 459-468
Experimentally observed germline mutations at human micro- and minisatellite loci
Authors: Sajantila, A Lukka, M Syvanen, AC
Citation: A. Sajantila et al., Experimentally observed germline mutations at human micro- and minisatellite loci, EUR J HUM G, 7(2), 1999, pp. 263-266
Coagulation factor V Leiden mutation in sudden fatal pulmonary embolism and in a general northern European population sample
Authors: Kuismanen, K Savontaus, ML Kozlov, A Vuorio, AF Sajantila, A
Citation: K. Kuismanen et al., Coagulation factor V Leiden mutation in sudden fatal pulmonary embolism and in a general northern European population sample, FOREN SCI I, 106(2), 1999, pp. 71-75
Post mortem molecularly defined familial hypercholesterolemia and sudden cardiac death of young men
Authors: Vuorio, AF Kontula, K Turtola, H Sajantila, A
Citation: Af. Vuorio et al., Post mortem molecularly defined familial hypercholesterolemia and sudden cardiac death of young men, FOREN SCI I, 106(2), 1999, pp. 87-92
mtDNA analysis of Nile River Valley populations: A genetic corridor or a barrier to migration
Authors: Krings, M Salem, AH Bauer, K Geisert, H Malek, AK Chaix, L Simon, C Welsby, D Di Rienzo, A Utermann, G Sajantila, A Paabo, S Stoneking, M
Citation: M. Krings et al., mtDNA analysis of Nile River Valley populations: A genetic corridor or a barrier to migration, AM J HU GEN, 64(4), 1999, pp. 1166-1176
Risultati: 1-15 |