A de novo POU3F3 Deletion in a Boy with Intellectual Disability and Dysmorphic Features

Publisher： Karger

E-ISSN： 1661-8777|5|1|32-35

ISSN： 1661-8769

Source： Molecular Syndromology, Vol.5, Iss.1, 2013-11, pp. : 32-35

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