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P Sistonen

Showing results (41-50 of 110) with videos related to

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Hereditas|June 17, 2000
MtDNA polymorphism in the Hungarians: comparison to three other Finno-Ugric-speaking populationsP Lahermo, V Laitinen, P Sistonen, et al.
Tissue Antigens|June 18, 1999
CD28/CTLA4 gene region on chromosome 2q33 confers genetic susceptibility to celiac disease. A linkage and family-based association studyP Holopainen, M Arvas, P Sistonen, et al.
Journal of Medical Genetics|April 22, 2008
Genome-wide linkage scan for loci of musical aptitude in Finnish families: evidence for a major locus at 4q22K Pulli, K Karma, R Norio, et al.
Nature Genetics|November 1, 1992
Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in FinlandJ Hästbacka, A de la Chapelle, I Kaitila, et al.
Blood|August 15, 1995
Molecular basis and expression of the LWa/LWb blood group polymorphismP Hermand, P Gane, M G Mattei, et al.
American Journal of Human Genetics|June 1, 1996
The genetic relationship between the Finns and the Finnish Saami (Lapps): analysis of nuclear DNA and mtDNAP Lahermo, A Sajantila, P Sistonen, et al.
Forensic Science International|March 6, 2007
Finnish mitochondrial DNA HVS-I and HVS-II population dataM Hedman, A Brandstätter, V Pimenoff, et al.
Genome Research|March 7, 2001
Y-chromosomal SNPs in Finno-Ugric-speaking populations analyzed by minisequencing on microarraysM Raitio, K Lindroos, M Laukkanen, et al.
Genomics|December 1, 1991
A linkage map spanning the locus for diastrophic dysplasia (DTD)J Hästbacka, P Sistonen, I Kaitila, et al.
European Journal of Human Genetics : EJHG|June 3, 1999
Y chromosomal polymorphisms reveal founding lineages in the Finns and the SaamiP Lahermo, M L Savontaus, P Sistonen, et al.
Pageof 11

Showing results (41-50 of 110) with videos related to

Sort By:
Pageof 11
Hereditas|June 17, 2000
MtDNA polymorphism in the Hungarians: comparison to three other Finno-Ugric-speaking populationsP Lahermo, V Laitinen, P Sistonen, et al.
Tissue Antigens|June 18, 1999
CD28/CTLA4 gene region on chromosome 2q33 confers genetic susceptibility to celiac disease. A linkage and family-based association studyP Holopainen, M Arvas, P Sistonen, et al.
Journal of Medical Genetics|April 22, 2008
Genome-wide linkage scan for loci of musical aptitude in Finnish families: evidence for a major locus at 4q22K Pulli, K Karma, R Norio, et al.
Nature Genetics|November 1, 1992
Linkage disequilibrium mapping in isolated founder populations: diastrophic dysplasia in FinlandJ Hästbacka, A de la Chapelle, I Kaitila, et al.
Blood|August 15, 1995
Molecular basis and expression of the LWa/LWb blood group polymorphismP Hermand, P Gane, M G Mattei, et al.
American Journal of Human Genetics|June 1, 1996
The genetic relationship between the Finns and the Finnish Saami (Lapps): analysis of nuclear DNA and mtDNAP Lahermo, A Sajantila, P Sistonen, et al.
Forensic Science International|March 6, 2007
Finnish mitochondrial DNA HVS-I and HVS-II population dataM Hedman, A Brandstätter, V Pimenoff, et al.
Genome Research|March 7, 2001
Y-chromosomal SNPs in Finno-Ugric-speaking populations analyzed by minisequencing on microarraysM Raitio, K Lindroos, M Laukkanen, et al.
Genomics|December 1, 1991
A linkage map spanning the locus for diastrophic dysplasia (DTD)J Hästbacka, P Sistonen, I Kaitila, et al.
European Journal of Human Genetics : EJHG|June 3, 1999
Y chromosomal polymorphisms reveal founding lineages in the Finns and the SaamiP Lahermo, M L Savontaus, P Sistonen, et al.
Pageof 11