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- 2017
-
Mark
Rare variant, gene-based association study of hereditary melanoma using whole-exome sequencing
(
- Contribution to journal › Article
- 2016
-
Mark
A reference panel of 64,976 haplotypes for genotype imputation
(
- Contribution to journal › Article
- 2014
-
Mark
Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population.
(
- Contribution to journal › Article