de Ceulaer, K <br/><br/>
alpha-Thalassemia reduces the hemolytic rate in homozygous sickle-cell disease.  [electronic resource] 

 -  The New England journal of medicine  Jul 1983 
 - 189-90 p.  digital 
<br/><br/> Publication Type: Letter 
<br/><br/><label>ISSN: </label>0028-4793 
<br/><br/><label>Standard No.: </label>10.1056/NEJM198307213090320  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Anemia, Sickle Cell--blood<br/>Erythrocyte Aging<br/>Female<br/>Hemolysis<br/>Homozygote<br/>Humans<br/>Male<br/>Thalassemia--blood