de Greef, J C <br/><br/>
Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHD.  [electronic resource] 

 -  Neurology  Sep 2007 
 - 1018-26 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1526-632X 
<br/><br/><label>Standard No.: </label>10.1212/01.wnl.0000271391.44352.fe  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Alleles<br/>Chromosomes, Human, Pair 4--genetics<br/>DNA Methylation<br/>Female<br/>Humans<br/>Male<br/>Middle Aged<br/>Muscular Dystrophy, Facioscapulohumeral--genetics<br/>Mutation<br/>Pedigree<br/>Phenotype<br/>Tandem Repeat Sequences--genetics