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Human Molecular Genetics
|
May 1, 1994
The sequence organization of the long arm pseudoautosomal region of the human sex chromosomes
K Kvaløy, F Galvagni, W R Brown
International Journal of Obesity (2005)
|
January 16, 2013
Sex-specific effects of weight-affecting gene variants in a life course perspective--The HUNT Study, Norway
K Kvaløy, B Kulle, P Romundstad, et al.
Diabetologia
|
February 3, 2012
Time dynamics of autoantibodies are coupled to phenotypes and add to the heterogeneity of autoimmune diabetes in adults: the HUNT study, Norway
E P Sørgjerd, F Skorpen, K Kvaløy, et al.
Genomics
|
September 15, 1996
Human uracil-DNA glycosylase gene: sequence organization, methylation pattern, and mapping to chromosome 12q23-q24.1
T Haug, F Skorpen, K Kvaløy, et al.
Genomics
|
March 15, 1997
Genetic polymorphism and recombination in the subtelomeric region of chromosome 14q
R F Wintle, T G Nygaard, J A Herbrick, et al.
Journal of Molecular Biology
|
March 20, 1993
Prokaryotic members of a new family of putative helicases with similarity to transcription activator SNF2
A B Kolstø, P Bork, K Kvaløy, et al.
Mutation Research
|
December 6, 2000
Sequence variation in the human uracil-DNA glycosylase (UNG) gene
K Kvaløy, H Nilsen, K S Steinsbekk, et al.
Current Microbiology
|
July 15, 1998
Genetic diversity of Bacillus cereus/B. thuringiensis isolates from natural sources
E Helgason, D A Caugant, M M Lecadet, et al.
Molecular Ecology
|
August 17, 2006
Population structure in a critically endangered arctic fox population: does genetics matter?
L Dalén, K Kvaløy, J D C Linnell, et al.
American Journal of Human Genetics
|
November 1, 1995
Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome
M Muenke, L J Bone, H F Mitchell, et al.
Page
of 2
Search research articles
Search
Showing results (1-10 of 11) with videos related to
Sort By:
Page
of 2
Human Molecular Genetics
|
May 1, 1994
The sequence organization of the long arm pseudoautosomal region of the human sex chromosomes
K Kvaløy, F Galvagni, W R Brown
International Journal of Obesity (2005)
|
January 16, 2013
Sex-specific effects of weight-affecting gene variants in a life course perspective--The HUNT Study, Norway
K Kvaløy, B Kulle, P Romundstad, et al.
Diabetologia
|
February 3, 2012
Time dynamics of autoantibodies are coupled to phenotypes and add to the heterogeneity of autoimmune diabetes in adults: the HUNT study, Norway
E P Sørgjerd, F Skorpen, K Kvaløy, et al.
Genomics
|
September 15, 1996
Human uracil-DNA glycosylase gene: sequence organization, methylation pattern, and mapping to chromosome 12q23-q24.1
T Haug, F Skorpen, K Kvaløy, et al.
Genomics
|
March 15, 1997
Genetic polymorphism and recombination in the subtelomeric region of chromosome 14q
R F Wintle, T G Nygaard, J A Herbrick, et al.
Journal of Molecular Biology
|
March 20, 1993
Prokaryotic members of a new family of putative helicases with similarity to transcription activator SNF2
A B Kolstø, P Bork, K Kvaløy, et al.
Mutation Research
|
December 6, 2000
Sequence variation in the human uracil-DNA glycosylase (UNG) gene
K Kvaløy, H Nilsen, K S Steinsbekk, et al.
Current Microbiology
|
July 15, 1998
Genetic diversity of Bacillus cereus/B. thuringiensis isolates from natural sources
E Helgason, D A Caugant, M M Lecadet, et al.
Molecular Ecology
|
August 17, 2006
Population structure in a critically endangered arctic fox population: does genetics matter?
L Dalén, K Kvaløy, J D C Linnell, et al.
American Journal of Human Genetics
|
November 1, 1995
Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome
M Muenke, L J Bone, H F Mitchell, et al.
Page
of 2