9q33.3q34.11 microdeletion: new contiguous gene syndrome encompassing STXBP1, LMX1B and ENG genes assessed using reverse phenotyping
European journal of human genetics : EJHG, 2016-06, Vol.24 (6), p.830-837 [Peer Reviewed Journal]Copyright Nature Publishing Group Jun 2016 ;Macmillan Publishers Limited 2016. ;Distributed under a Creative Commons Attribution 4.0 International License ;Copyright © 2016 Macmillan Publishers Limited 2016 Macmillan Publishers Limited ;ISSN: 1018-4813 ;EISSN: 1476-5438 ;DOI: 10.1038/ejhg.2015.202 ;PMID: 26395556
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