CORE
🇺🇦
make metadata, not war
Services
Services overview
Explore all CORE services
Access to raw data
API
Dataset
FastSync
Content discovery
Recommender
Discovery
OAI identifiers
OAI Resolver
Managing content
Dashboard
Bespoke contracts
Consultancy services
Support us
Support us
Membership
Sponsorship
Community governance
Advisory Board
Board of supporters
Research network
About
About us
Our mission
Team
Blog
FAQs
Contact us
Whole-genome sequencing identifies rare genotypes in <em>COMP</em> and <em>CHADL</em> associated with high risk of hip osteoarthritis
Authors
Agustsdottir AB
Almdahl IS
+47 more
Andreassen OA
arcOGEN consortium
Azizi F
Braund PS
Brækhus A
Christiansen C
Danesphour M
Fladby T
Gretarsdottir S
Gudbjartsson D
Halldorsson GH
Helgadottir A
Helgason A
Helgason H
Hosseinpana F
Ingvarsson T
Johannsdottir HS
Jonasdottir A
Jonsdottir I
Jonsson H
Kiemeney LA
Koh JM
Kong A
Lohmander LS
Loughlin J
Magnusdottir A
Magnusson O
Masson G
Mayordomo JI
Norddahl GL
Oddson A
Rafnar T
Reynard LN
Samani NJ
Selbæk G
Sigurdsson A
Stefansson H
Stefansson K
Styrkarsdottir U
Sulem G
Sulem P
Sveinbjornsson G
Tang NL
Thorsteinsdottir U
Villalvilla A
Welt C
Zink F
Publication date
Publisher
Nature Publishing Group
Abstract
Abstract is not available.
Similar works
Full text
Available Versions
Newcastle University E-Prints
See this paper in CORE
Go to the repository landing page
Download from data provider
oai:eprints.ncl.ac.uk:233263
Last time updated on 30/05/2021