Klinge, Lars <br/><br/>
Severe phenotype in infantile facioscapulohumeral muscular dystrophy.  [electronic resource] 

 -  Neuromuscular disorders : NMD  Oct 2006 
 - 553-8 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0960-8966 
<br/><br/><label>Standard No.: </label>10.1016/j.nmd.2006.06.008  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Child<br/>Cohort Studies<br/>DNA Mutational Analysis<br/>Disease Progression<br/>Female<br/>Genetic Predisposition to Disease--genetics<br/>Genetic Testing<br/>Humans<br/>Inheritance Patterns--genetics<br/>Longitudinal Studies<br/>Lordosis--genetics<br/>Male<br/>Mosaicism<br/>Muscle Weakness--genetics<br/>Muscle, Skeletal--metabolism<br/>Muscular Atrophy--genetics<br/>Muscular Dystrophy, Facioscapulohumeral--diagnosis<br/>Mutation--genetics<br/>Phenotype<br/>Prognosis<br/>Sex Distribution