DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

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

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