A Boy with an LCR3/4-Flanked 10q22.3q23.2 Microdeletion and Uncommon Phenotypic Features

Publisher： Karger

E-ISSN： 1661-8777|5|1|19-24

ISSN： 1661-8769

Source： Molecular Syndromology, Vol.5, Iss.1, 2013-11, pp. : 19-24

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