Lim, Derek Hk <br/><br/>
Human imprinting syndromes.  [electronic resource] 

 -  Epigenomics  Dec 2009 
 - 347-69 p.  digital 
<br/><br/> Publication Type: Journal Article; Review 
<br/><br/><label>ISSN: </label>1750-192X 
<br/><br/><label>Standard No.: </label>10.2217/epi.09.24  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adaptor Proteins, Signal Transducing--genetics<br/>Angelman Syndrome--genetics<br/>Beckwith-Wiedemann Syndrome--genetics<br/>Chromosome Disorders--genetics<br/>Chromosomes, Human, Pair 11--genetics<br/>Chromosomes, Human, Pair 14--genetics<br/>Chromosomes, Human, Pair 15--genetics<br/>Chromosomes, Human, Pair 20--genetics<br/>Chromosomes, Human, Pair 6--genetics<br/>Diabetes Mellitus--genetics<br/>Female<br/>Fibrous Dysplasia, Polyostotic--genetics<br/>Genomic Imprinting--physiology<br/>Humans<br/>Hydatidiform Mole--genetics<br/>Multigene Family--genetics<br/>Mutation--genetics<br/>Prader-Willi Syndrome--genetics<br/>Pregnancy<br/>Pseudohypoparathyroidism--genetics<br/>Silver-Russell Syndrome--genetics<br/>Uniparental Disomy--genetics