Fidzianska, A <br/><br/>
An X:autosome translocation stabilizes truncated dystrophin: implications for lack of truncated dystrophins in Duchenne muscular dystrophy.  [electronic resource] 

 -  Neuropediatrics  Jun 1995 
 - 163-7 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0174-304X 
<br/><br/><label>Standard No.: </label>10.1055/s-2007-979747  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Antibodies, Monoclonal<br/>Child, Preschool<br/>Chromosomes, Human, Pair 22<br/>Dystrophin--genetics<br/>Female<br/>Gene Amplification<br/>Humans<br/>Immunoblotting<br/>Immunohistochemistry<br/>Muscles--chemistry<br/>Muscular Dystrophies--genetics<br/>Polymerase Chain Reaction<br/>RNA<br/>Translocation, Genetic<br/>X Chromosome