Fontana, L <br/><br/>
Characterization of multi-locus imprinting disturbances and underlying genetic defects in patients with chromosome 11p15.5 related imprinting disorders.  [electronic resource] 

 -  Epigenetics  2018 
 - 897-909 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1559-2308 
<br/><br/><label>Standard No.: </label>10.1080/15592294.2018.1514230  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adaptor Proteins, Signal Transducing--chemistry<br/>Adolescent<br/>Apoptosis Regulatory Proteins<br/>Beckwith-Wiedemann Syndrome--genetics<br/>Child<br/>Child, Preschool<br/>Chromosomes, Human, Pair 15--genetics<br/>DNA Methylation<br/>Female<br/>Genomic Imprinting<br/>Humans<br/>Infant<br/>Kruppel-Like Transcription Factors--chemistry<br/>Male<br/>Mutation, Missense<br/>Silver-Russell Syndrome--genetics<br/>Young Adult