Stefanis, L <br/><br/>
Hematologic phenotype of the mutations IVS1-n6 (T-->C), IVS1-n110 (G-->A), and CD39 (C-->T) in carriers of beta-thalassemia in Greece.  [electronic resource] 

 -  Pediatric hematology and oncology   
 - 509-17 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0888-0018 
<br/><br/><label>Standard No.: </label>10.3109/08880019409141689  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Erythrocyte Indices<br/>Female<br/>Fetal Hemoglobin--analysis<br/>Globins--genetics<br/>Greece<br/>Hematocrit<br/>Hemoglobin A2--analysis<br/>Heterozygote<br/>Humans<br/>Male<br/>Phenotype<br/>Point Mutation<br/>beta-Thalassemia--blood