Shaheen, R <br/><br/>
Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs.  [electronic resource] 

 -  Clinical genetics  Jan 2011 
 - 60-70 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2010.01498.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Arabs<br/>Child, Preschool<br/>Cytogenetic Analysis<br/>Female<br/>Genetic Association Studies<br/>Genetic Heterogeneity<br/>Humans<br/>Infant<br/>Infant, Newborn<br/>Male<br/>Middle East<br/>Mutation<br/>Peroxisomal Disorders--ethnology<br/>Peroxisomes--genetics<br/>Sequence Analysis