DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
LinksClose Window
References
Ma D, Wang X, Guo J, Zhang J, Cai T.
Identification of a novel mutation of RUNX2 in a family with supernumerary teeth and craniofacial dysplasia by whole-exome sequencing: a case report and literature review.
Medicine (Baltimore) 2018;
97 (32) e11328
We do not assume any responsibility for the contents of the web pages of other providers.