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Works matching AU Seppälä, E. H.

Results: 3

1

CHEK2 variants associate with hereditary prostate cancer.

Published in:

British Journal of Cancer, 2003, v. 89, n. 10, p. 1966, doi. 10.1038/sj.bjc.6601425

By:

Seppälä, E. H.;
Ikonen, T.;
Mononen, N.;
Autio, V.;
Rökman, A.;
Matikainen, M. P.;
Tammela, T. L. J.;
Schleutker, J.

Publication type:

Article

2

Assessment of the functionality of genome-wide canine SNP arrays and implications for canine disease association studies.

Published in:

Animal Genetics, 2011, v. 42, n. 2, p. 181, doi. 10.1111/j.1365-2052.2010.02132.x

By:

Ke, X.;
Kennedy, L. J.;
Short, A. D.;
Seppälä, E. H.;
Barnes, A.;
Clements, D. N.;
Wood, S. H.;
Carter, S. D.;
Happ, G. M.;
Lohi, H.;
Ollier, W. E. R.

Publication type:

Article

3

Regional occurrence, high frequency but low diversity of mitochondrial DNA haplogroup d1 suggests a recent dog-wolf hybridization in Scandinavia.

Published in:

Animal Genetics, 2011, v. 42, n. 1, p. 100, doi. 10.1111/j.1365-2052.2010.02069.x

By:

Klütsch, C. F. C.;
Seppälä, E. H.;
Fall, T.;
Uhlén, M.;
Hedhammar, Å.;
Lohi, H.;
Savolainen, P.

Publication type:

Article