Niemi, Anna-Kaisa <br/><br/>
Report of two patients and further characterization of interstitial 9p13 deletion--a rare but recurrent microdeletion syndrome?  [electronic resource] 

 -  American journal of medical genetics. Part A  Sep 2012 
 - 2328-35 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.35536  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Chromosome Deletion<br/>Chromosomes, Human, Pair 9<br/>Female<br/>Humans<br/>Infant, Newborn<br/>Male