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PDFDevelopmental defects
Original article
A specific mutation in TBL1XR1 causes Pierpont syndrome
- Correspondence to Dr Raoul C Hennekam, Department of Paediatrics, H7-236, Academic Medical Centre, P.O. Box 22660, Amsterdam 1100 DD, The Netherlands; r.c.hennekam{at}amc.uva.nl
Citation
A specific mutation in TBL1XR1 causes Pierpont syndrome
Publication history
- Received May 1, 2015
- Revised December 10, 2015
- Accepted December 14, 2015
- First published January 14, 2016.
Online issue publication
May 24, 2016
Article Versions
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Supplementary Data
This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.
- Data supplement 1 - Online supplement
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Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/