Taşdemir, H A <br/><br/>
Correlation of laboratory and clinical findings with the location of Xp21 deletion in Duchenne muscular dystrophy.  [electronic resource] 

 -  The Turkish journal of pediatrics   
 - 317-24 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>0041-4301 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Child, Preschool<br/>Dwarfism--genetics<br/>Dystrophin--genetics<br/>Exons<br/>Humans<br/>Muscular Dystrophies--complications<br/>Regression Analysis<br/>Sequence Deletion<br/>Severity of Illness Index