Article info
Cancer genetics
Short report
Acute myeloid leukaemia in a case with Tatton-Brown-Rahman syndrome: the peculiar DNMT3A R882 mutation
- Correspondence to Iris H I M Hollink, Department of Clinical Genetics, Erasmus Medical Center, P.O. Box 2040, 3000 CA Rotterdam, The Netherlands; i.hollink{at}erasmusmc.nl
Citation
Acute myeloid leukaemia in a case with Tatton-Brown-Rahman syndrome: the peculiar DNMT3A R882 mutation
Publication history
- Received January 30, 2017
- Revised March 21, 2017
- Accepted March 22, 2017
- First published April 21, 2017.
Online issue publication
November 23, 2017
Article Versions
- Previous version (21 April 2017).
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© Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2017. All rights reserved. No commercial use is permitted unless otherwise expressly granted.