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

Publisher： John Wiley & Sons Inc

E-ISSN： 1552-4833|167|6|1315-1322

ISSN： 1552-4825

Source： American Journal Of Medical Genetics Part A, Vol.167, Iss.6, 2015-06, pp. : 1315-1322

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