Ramelli, G P <br/><br/>
Becker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series.  [electronic resource] 

 -  Swiss medical weekly  Mar 2006 
 - 189-93 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1424-7860 
<br/><br/><label>Standard No.: </label>10.4414/smw.2006.11213  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Child<br/>Creatine Kinase--analysis<br/>Dystrophin--genetics<br/>Genotype<br/>Humans<br/>Molecular Biology<br/>Muscular Dystrophy, Duchenne--diagnosis<br/>Pathology, Clinical<br/>Phenotype<br/>Switzerland