Qin, Xue-Yan <br/><br/>
Novel Mutation of Cleidocranial Dysplasia-related Frameshift Runt-related Transcription Factor 2 in a Sporadic Chinese Case.  [electronic resource] 

 -  Chinese medical journal  01 2017 
 - 165-170 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>2542-5641 
<br/><br/><label>Standard No.: </label>10.4103/0366-6999.197996  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Cell Nucleus--metabolism<br/>Cleidocranial Dysplasia--genetics<br/>Core Binding Factor Alpha 1 Subunit--genetics<br/>Female<br/>Frameshift Mutation--genetics<br/>Humans<br/>Microscopy, Fluorescence<br/>Mutation