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2023
Mark Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
Oddsson, Asmundur ; Sulem, Patrick ; Sveinbjornsson, Gardar ; Arnadottir, Gudny A ; Steinthorsdottir, Valgerdur ; Halldorsson, Gisli H ; Atlason, Bjarni A ; Oskarsson, Gudjon R ; Helgason, Hannes and Nielsen, Henriette Svarre , et al. (2023) In Nature Communications 14(1). p.3453-3453
- Contribution to journal › Article
2017
Mark Whole-genome sequencing identifies rare genotypes in COMP and CHADL associated with high risk of hip osteoarthritis
Styrkarsdottir, Unnur ; Helgason, Hannes ; Sigurdsson, Asgeir ; Norddahl, Gudmundur L. ^LU ; Agustsdottir, Arna B. ; Reynard, Louise N. ; Villalvilla, Amanda ; Halldorsson, Gisli H. ; Jonasdottir, Aslaug and Magnusdottir, Audur , et al. (2017) In Nature Genetics 49(5). p.801-805
- Contribution to journal › Article

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