CORE
🇺🇦Â
 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
Genetic diagnosis of monogenic or polygenic Familial Hypercholesterolemia in Northern Ireland: Evaluation of the Randox FH Arrays in combination with the Randox 6SNP Polygenic Hypercholesterolemia Array
Authors
Deborah Bailie
M Crockard
+10Â more
S Fitzgerald
Colin Graham
Paul Hamilton
Padraig Hart
J Lamont
M Latten
H McMillan
H Murray
Christopher Patterson
Ian Young
Publication date
1 January 2017
Publisher
Abstract
Abstract is not available.
Similar works
Full text
Available Versions
Supporting member
Queen's University Belfast Research Portal
See this paper in CORE
Go to the repository landing page
Download from data provider
oai:pure.qub.ac.uk/portal:publ...
Last time updated on 06/11/2019
