Eggermann, Thomas <br/><br/>
CDKN1C mutations: two sides of the same coin.  [electronic resource] 

 -  Trends in molecular medicine  Nov 2014 
 - 614-22 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Review 
<br/><br/><label>ISSN: </label>1471-499X 
<br/><br/><label>Standard No.: </label>10.1016/j.molmed.2014.09.001  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adrenal Insufficiency--diagnosis<br/>Animals<br/>Beckwith-Wiedemann Syndrome--diagnosis<br/>Chromosome Aberrations<br/>Chromosomes, Human, Pair 11<br/>Cyclin-Dependent Kinase Inhibitor p57--genetics<br/>Disease Management<br/>Fetal Growth Retardation--diagnosis<br/>Genetic Association Studies<br/>Genetic Counseling<br/>Genomic Imprinting<br/>Humans<br/>Mutation<br/>Osteochondrodysplasias--diagnosis<br/>Urogenital Abnormalities--diagnosis