Rozas, M Fernanda <br/><br/>
Association between phenotype and deletion size in 22q11.2 microdeletion syndrome: systematic review and meta-analysis.  [electronic resource] 

 -  Orphanet journal of rare diseases  08 2019 
 - 195 p.  digital 
<br/><br/> Publication Type: Journal Article; Meta-Analysis; Research Support, Non-U.S. Gov't; Review; Systematic Review 
<br/><br/><label>ISSN: </label>1750-1172 
<br/><br/><label>Standard No.: </label>10.1186/s13023-019-1170-x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Arachnodactyly--genetics<br/>Chromosome Deletion<br/>Craniosynostoses--genetics<br/>Humans<br/>Marfan Syndrome--genetics<br/>Phenotype