Massaad, E <br/><br/>
Char Syndrome a novel mutation and new insights: A clinical report.  [electronic resource] 

 -  European journal of medical genetics  Dec 2019 
 - 103607 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1878-0849 
<br/><br/><label>Standard No.: </label>10.1016/j.ejmg.2018.12.012  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Ductus Arteriosus, Patent--genetics<br/>Face--abnormalities<br/>Fingers--abnormalities<br/>Humans<br/>Infant<br/>Male<br/>Mutation<br/>Phenotype<br/>Transcription Factor AP-2--genetics