Netchine, Irčne <br/><br/>
11p15 imprinting center region 1 loss of methylation is a common and specific cause of typical Russell-Silver syndrome: clinical scoring system and epigenetic-phenotypic correlations.  [electronic resource] 

 -  The Journal of clinical endocrinology and metabolism  Aug 2007 
 - 3148-54 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0021-972X 
<br/><br/><label>Standard No.: </label>10.1210/jc.2007-0354  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Aging--metabolism<br/>Chromosomes, Human, Pair 7--genetics<br/>DNA--genetics<br/>Face--abnormalities<br/>Female<br/>Fetal Growth Retardation--genetics<br/>Genomic Imprinting<br/>Humans<br/>Infant, Newborn<br/>Infant, Small for Gestational Age--physiology<br/>Insulin-Like Growth Factor II--metabolism<br/>Male<br/>Methylation<br/>Mutation--genetics<br/>Phenotype<br/>Syndrome