Article info
PDFCancer genetics
Review
Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancy
- Correspondence to Dr Katharina Wimmer, Division of Human Genetics, Medical University Innsbruck, Innsbruck 6020, Austria; katharina.wimmer{at}i-med.ac.at
Citation
Constitutional mismatch repair deficiency as a differential diagnosis of neurofibromatosis type 1: consensus guidelines for testing a child without malignancy
Publication history
- Received August 6, 2018
- Revised October 5, 2018
- Accepted October 10, 2018
- First published November 10, 2018.
Online issue publication
January 22, 2019
Article Versions
- Previous version (10 November 2018).
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© Author(s) (or their employer(s)) 2019. No commercial re-use. See rights and permissions. Published by BMJ.