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Acute myeloid leukaemia in a case with Tatton-Brown-Rahman syndrome: the peculiar DNMT3A R882 mutation

Authors

  1. 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
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Citation

Hollink IHIM, van den Ouweland AMW, Beverloo HB, et al
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

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