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A Korean family with KBG syndrome identified by ANKRD11 mutation, and phenotypic comparison of ANKRD11 mutation and 16q24.3 microdeletion

Author:

Hyo Jeong Kim,Eunhae Cho,Jong Bum Park,Woo Young Im,Hyon J. Kim

Publication:

European Journal of Medical Genetics

Publisher:

Elsevier

Date:

February 2015

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