Hickey, Scott E <br/><br/>
Multigeneration family with short stature, developmental delay, and dysmorphic features due to 4q27-q28.1 microdeletion.  [electronic resource] 

 -  European journal of medical genetics  Sep 2013 
 - 521-5 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.2013.07.004  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--diagnosis<br/>Adult<br/>Child<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 4--genetics<br/>Developmental Disabilities--diagnosis<br/>Female<br/>Growth Disorders--diagnosis<br/>Humans<br/>Infant, Newborn<br/>Male<br/>Pedigree<br/>Syndrome