Yu, Andrea C <br/><br/>
Variable developmental delays and characteristic facial features-A novel 7p22.3p22.2 microdeletion syndrome?  [electronic resource] 

 -  American journal of medical genetics. Part A  Jun 2017 
 - 1593-1600 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.38241  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child, Preschool<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 7--genetics<br/>DNA Copy Number Variations--genetics<br/>Developmental Disabilities--genetics<br/>Female<br/>Humans<br/>Infant<br/>Male<br/>Monosomy