Bartholdi, D <br/><br/>
Epigenetic mutations of the imprinted IGF2-H19 domain in Silver-Russell syndrome (SRS): results from a large cohort of patients with SRS and SRS-like phenotypes.  [electronic resource] 

 -  Journal of medical genetics  Mar 2009 
 - 192-7 p.  digital 
<br/><br/> Publication Type: Letter; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.2008.061820  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adolescent<br/>Adult<br/>Analysis of Variance<br/>Child<br/>Child, Preschool<br/>Cohort Studies<br/>Craniofacial Abnormalities--genetics<br/>DNA Methylation<br/>Epigenesis, Genetic<br/>Female<br/>Fetal Growth Retardation--genetics<br/>Genomic Imprinting<br/>Humans<br/>Infant<br/>Insulin-Like Growth Factor II--genetics<br/>Male<br/>Mutation<br/>Phenotype<br/>Pregnancy<br/>Research Design<br/>Syndrome<br/>Uniparental Disomy