Molecular Basis of α-Thalassemia in Algeria
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.1080/03630260802004301
Reference22 articles.
1. Hemoglobin Bart’s in Northern Algeria
2. ?-Thalassemia haplotypes in the Algerian population
3. Identification of three different α-thalassemic haplotypes: —α3.7, (— —)MED and αHph α in the same Algerian family
4. Human α‐Thalassemia syndromes: Detection of molecular defects
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