Functional analysis of novel RUNX2 mutations identified in patients with Cleidocranial dysplasia.

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Source: Clinical Genetics - July 25, 2019 Category: Genetics & Stem Cells Authors: Hordyjewska-Kowalczyk E, SowiŃska-Seidler A, Olech EM, Socha M, Glazar R, Kruczek A, Latos-BieleŃska A, Tylzanowski P, Jamsheer A Tags: Clin Genet Source Type: research