Parano, E <br/><br/>
Molecular basis of phenotypic heterogeneity in siblings with spinal muscular atrophy.  [electronic resource] 

 -  Annals of neurology  Aug 1996 
 - 247-51 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0364-5134 
<br/><br/><label>Standard No.: </label>10.1002/ana.410400219  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Child, Preschool<br/>Electromyography<br/>Family<br/>Female<br/>Gene Deletion<br/>Genetic Variation<br/>Humans<br/>Male<br/>Phenotype<br/>Polymerase Chain Reaction<br/>Polymorphism, Genetic--genetics<br/>Spinal Muscular Atrophies of Childhood--diagnosis