Article info
Position statement
Rare disease genomic testing in the UK and Ireland: promoting timely and equitable access
- Correspondence to Prof Emma L Baple; ebaple{at}nhs.net; Prof Robert W Taylor; robert.taylor{at}newcastle.ac.uk
Citation
Rare disease genomic testing in the UK and Ireland: promoting timely and equitable access
Publication history
- Received July 9, 2024
- Accepted September 9, 2024
- First published September 26, 2024.
Article Versions
- Previous version (26 September 2024).
- You are viewing the most recent version of this article.
Supplementary Data
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Supplementary Data
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
Request permissions
If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Copyright information
© Author(s) (or their employer(s)) 2024. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.