This shareable PDF can be hosted on any platform or network and is fully compliant with publisher copyright.
This publication has not yet been explained in plain language by the author(s). However, you can still read the publication.
If you are one of the authors, claim this publication so you can create a plain language summary to help more people find, understand and use it.
This page is a summary of: The clinical heterogeneity of
RUNX1
associated familial platelet disorder with predisposition to myeloid malignancy – A case series and review of the literature, Research and Practice in Thrombosis and Haemostasis, December 2019, Wiley,
DOI: 10.1002/rth2.12282.
You can read the full text:
The following have contributed to this page
