Harteveld, Cornelis L <br/><br/>
alpha-thalassaemia masked by beta gene defects and a new polyadenylation site mutation on the alpha2-globin gene.  [electronic resource] 

 -  European journal of haematology  Apr 2010 
 - 354-8 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1600-0609 
<br/><br/><label>Standard No.: </label>10.1111/j.1600-0609.2009.01380.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Female<br/>Hemoglobins, Abnormal--genetics<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Middle Aged<br/>Mutation<br/>RNA 3' Polyadenylation Signals--genetics<br/>alpha-Globins--genetics<br/>alpha-Thalassemia--diagnosis<br/>beta-Globins--genetics<br/>beta-Thalassemia--genetics