Zhang, Tingting <br/><br/>
Whole-exome sequencing identification of a novel splicing mutation of RUNX2 in a Chinese family with cleidocranial dysplasia.  [electronic resource] 

 -  Archives of oral biology  Apr 2019 
 - 49-56 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1879-1506 
<br/><br/><label>Standard No.: </label>10.1016/j.archoralbio.2019.02.005  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Asian People<br/>Cleidocranial Dysplasia--genetics<br/>Core Binding Factor Alpha 1 Subunit--genetics<br/>Humans<br/>Mutation<br/>Protein Splicing<br/>RNA Splice Sites<br/>Exome Sequencing