Molecular characterization of sickle cell anemia in the Northern Brazilian state of Pará
Author:
Publisher
Wiley
Subject
Genetics,Anthropology,Ecology, Evolution, Behavior and Systematics,Anatomy
Reference46 articles.
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3. β-Thalassemia and sickle cell anemia as paradigms of hypercoagulability;Ataga;Br J Haematol,2007
4. Hematological phenotype and the type of β-thalassemia mutation in Brazil;Bertuzzo;Braz J Genet,1997
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1. Alpha thalassemia, but not βS-globin haplotypes, influence sickle cell anemia clinical outcome in a large, single-center Brazilian cohort;Annals of Hematology;2021-02-13
2. Relationships among genomic ancestry, clinical manifestations, socioeconomic status, and skin color of people with sickle cell disease in the State of Pará, Amazonia, Brazil;Antropologia Portuguesa;2020-12-11
3. Influence of alpha thalassemia on clinical and laboratory parameters among nigerian children with sickle cell anemia;Journal of Clinical Laboratory Analysis;2018-08-20
4. Mutational Profile of Homozygousβ-Thalassemia in Rio de Janeiro, Brazil;Hemoglobin;2017-01-02
5. Genetic modulators of sickle cell disease in French Guiana: Markers of the slave trade;American Journal of Human Biology;2016-06-02
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