2015. Feb
A Korean family with KBG syndrome identified by ANKRD11 mutation, and phenotypic comparison of ANKRD11 mutation and 16q24.3 microdeletion.
Eur J Med Genet. 2015
Kim HJ, Cho E, Park JB, Im WY, Kim HJ.
A Korean family with KBG syndrome identified by ANKRD11 mutation, and phenotypic comparison of ANKRD11 mutation and 16q24.3 microdeletion.
Eur J Med Genet. 2015
Kim HJ, Cho E, Park JB, Im WY, Kim HJ.