Müller, Anne <br/><br/>
No major contribution of IGF2 variants to the etiology of sporadic 11p15-associated imprinting disorders.  [electronic resource] 

 -  American journal of medical genetics. Part A  Jan 2016 
 - 283-4 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1552-4833 
<br/><br/><label>Standard No.: </label>10.1002/ajmg.a.37416  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Beckwith-Wiedemann Syndrome--genetics<br/>Chromosomes, Human, Pair 11--genetics<br/>Fetal Growth Retardation--genetics<br/>Genetic Testing<br/>Genomic Imprinting--genetics<br/>Humans<br/>Insulin-Like Growth Factor II--genetics