Pikó, Henriett <br/><br/>
[Role of associated alleles and hypomethylation status in the clinical expression of facioscapulohumeral muscular dystrophy].  [electronic resource] 

 -  Orvosi hetilap  Sep 2011 
 - 1576-85 p.  digital 
<br/><br/> Publication Type: English Abstract; Journal Article 
<br/><br/><label>ISSN: </label>0030-6002 
<br/><br/><label>Standard No.: </label>10.1556/OH.2011.29179  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Blotting, Southern<br/>Chromosomes, Human, Pair 4--genetics<br/>DNA Methylation<br/>Epigenesis, Genetic<br/>Humans<br/>Muscular Dystrophy, Facioscapulohumeral--genetics<br/>Phenotype<br/>Repetitive Sequences, Nucleic Acid<br/>Telomere--genetics