Article info
PDFDevelopmental defects
Communication
A protein-truncating mutation in CCNB3 in a patient with recurrent miscarriages and failure of meiosis I
- Correspondence to Dr Rima Slim, Human Genetics, Research Institute of the McGill University Health Centre, Montreal, Quebec H3A 0G4, Canada; rima.slim{at}muhc.mcgill.ca
Citation
A protein-truncating mutation in CCNB3 in a patient with recurrent miscarriages and failure of meiosis I
Publication history
- Received March 25, 2021
- Revised April 26, 2021
- Accepted May 6, 2021
- First published May 21, 2021.
Online issue publication
May 20, 2022
Article Versions
- Previous version (21 May 2021).
- You are viewing the most recent version of this article.
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)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.