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Deficit of homozygosity among 1.52 million individuals and ..:
Oddsson, Asmundur
;
Sulem, Patrick
;
Sveinbjornsson, Gardar
...
Nature Communications, 2023, 14:1,. , 2023
Link:
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-21178
RT Journal T1
Deficit of homozygosity among 1.52 million individuals and genetic causes of recessive lethality
UL https://suche.suub.uni-bremen.de/peid=base-ftumeauniv:oai:DiVA.org:umu-211785&Exemplar=1&LAN=DE A1 Oddsson, Asmundur A1 Sulem, Patrick A1 Sveinbjornsson, Gardar A1 Arnadottir, Gudny A A1 Steinthorsdottir, Valgerdur A1 Halldorsson, Gisli H A1 Atlason, Bjarni A A1 Oskarsson, Gudjon R A1 Helgason, Hannes A1 Nielsen, Henriette Svarre A1 Westergaard, David A1 Karjalainen, Juha M A1 Katrinardottir, Hildigunnur A1 Fridriksdottir, Run A1 Jensson, Brynjar O A1 Tragante, Vinicius A1 Ferkingstad, Egil A1 Jonsson, Hakon A1 Gudjonsson, Sigurjon A A1 Beyter, Doruk A1 Moore, Kristjan H. S A1 Thordardottir, Helga B A1 Kristmundsdottir, Snaedis A1 Stefansson, Olafur A A1 Rantapää-Dahlqvist, Solbritt A1 Sonderby, Ida Elken A1 Didriksen, Maria A1 Stridh, Pernilla A1 Haavik, Jan A1 Tryggvadottir, Laufey A1 Frei, Oleksandr A1 Walters, G. Bragi A1 Kockum, Ingrid A1 Hjalgrim, Henrik A1 Olafsdottir, Thorunn A A1 Selbaek, Geir A1 Nyegaard, Mette A1 Erikstrup, Christian A1 Brodersen, Thorsten A1 Saevarsdottir, Saedis A1 Olsson, Tomas A1 Nielsen, Kaspar Rene A1 Haraldsson, Asgeir A1 Bruun, Mie Topholm A1 Hansen, Thomas Folkmann A1 Brunak, Søren A1 Nielsen, Kasper Rene A1 Brun, Mie Topholm A1 Gudbjartsson, Daniel A1 Stefánsson, Hreinn A1 Þorsteinsdóttir, Unnur A1 Steingrimsdottir, Thora A1 Jacobsen, Rikke Louise A1 Lie, Rolv T A1 Djurovic, Srdjan A1 Alfredsson, Lars A1 Lopez de Lapuente Portilla, Aitzkoa A1 Brunak, Soren A1 Melsted, Pall A1 Halldorsson, Bjarni V A1 Saemundsdottir, Jona A1 Magnusson, Olafur Th A1 Padyukov, Leonid A1 Banasik, Karina A1 Rafnar, Thorunn A1 Askling, Johan A1 Klareskog, Lars A1 Pedersen, Ole Birger A1 Masson, Gisli A1 Havdahl, Alexandra A1 Nilsson, Bjorn A1 Andreassen, Ole A A1 Daly, Mark A1 Ostrowski, Sisse Rye A1 Jonsdottir, Ingileif A1 Holm, Hilma A1 Helgason, Agnar A1 Thorsteinsdottir, Unnur A1 Stefansson, Kari A1 Gudbjartsson, Daniel F PB Umeå universitet, Reumatologi; deCODE genetics/Amgen, Inc., Reykjavik, Iceland; deCODE genetics/Amgen, Inc., Reykjavik, Iceland; Faculty of Medicine, School of Health Sciences, University of Iceland, Reykjavik, Iceland; Deptartment of Obstetrics and Gynecology, Copenhagen University Hospital, Hvidovre, Denmark; Department of Clinical Medicine, Faculty of Health, University of Copenhagen, Copenhagen, Denmark; Deptartment of Obstetrics and Gynecology, Copenhagen University Hospital, Hvidovre, Denmark; Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark; Methods and Analysis, Statistics Denmark, Copenhagen, Denmark; Institute for Molecular Medicine, Finland, University of Helsinki, Helsinki, Finland; deCODE genetics/Amgen, Inc., Reykjavik, Iceland; Department of Anthropology, University of Iceland, Reykjavik, Iceland; Department of Medical Genetics, Oslo University Hospital and Univers... YR 2023 K1 Medical Genetics K1 Medicinsk genetik JF Nature Communications, 2023, 14:1, LK http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-211785 DO http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-211785 SF ELIB - SuUB Bremen
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