A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features
Identifiers
Identifiers
URI: http://hdl.handle.net/20.500.11940/2123
PMID: 25847113
DOI: 10.1002/ajmg.a.36909
ISSN: 1552-4825
Date issued
2015Journal title
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Type of content
Artigo