Rumaney, Maryam Bibi <br/><br/>
The co-inheritance of alpha-thalassemia and sickle cell anemia is associated with better hematological indices and lower consultations rate in Cameroonian patients and could improve their survival.  [electronic resource] 

 -  PloS one  2014 
 - e100516 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1932-6203 
<br/><br/><label>Standard No.: </label>10.1371/journal.pone.0100516  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Age Factors<br/>Anemia, Sickle Cell--blood<br/>Blood Cell Count<br/>Cameroon<br/>Female<br/>Gene Deletion<br/>Haplotypes<br/>Hemoglobin A--genetics<br/>Hemoglobin, Sickle--genetics<br/>Humans<br/>Inheritance Patterns<br/>Male<br/>Multigene Family<br/>Polymorphism, Single Nucleotide<br/>Referral and Consultation--statistics & numerical data<br/>Survival Analysis<br/>alpha-Globins--genetics<br/>alpha-Thalassemia--blood<br/>beta-Globins--genetics