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
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Identificadores![](/xmlui/themes/Mirage2//images/despl_identif.png)
Identificadores
URI: http://hdl.handle.net/20.500.11940/2123
PMID: 25847113
DOI: 10.1002/ajmg.a.36909
ISSN: 1552-4825
Fecha de publicación
2015Título de revista
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
Tipo de contenido
Artigo
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