Eggermann, Thomas <br/><br/>
Congenital imprinting disorders: a novel mechanism linking seemingly unrelated disorders.  [electronic resource] 

 -  The Journal of pediatrics  Oct 2013 
 - 1202-7 p.  digital 
<br/><br/> Publication Type: Clinical Conference; Journal Article 
<br/><br/><label>ISSN: </label>1097-6833 
<br/><br/><label>Standard No.: </label>10.1016/j.jpeds.2013.05.017  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Adolescent<br/>Child<br/>Child, Preschool<br/>Chromosome Mapping<br/>DNA Methylation<br/>Epigenesis, Genetic<br/>Female<br/>Genetic Association Studies<br/>Genomic Imprinting<br/>Heterozygote<br/>Humans<br/>Infant<br/>Male<br/>Phenotype<br/>Syndrome<br/>Uniparental Disomy--genetics