MIKOBI, T. M.; LUKUSA, P. T. HOMOZYGOUS DELETION ALFA-THALASSEMIA AND HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN, TWO GENETIC FACTORS PREDICTIVE THE REDUCTION OF MORBIDITY AND MORTALITY DURING PREGNANCY IN SICKLE CELL PATIENTS . A REPORT FROM DEMOCRATIC REPUBLIC OF CONGO: ALPHA THALASSEMIA AND HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN REDUCE MORBIDITY DURING PREGNANCY IN SICKLE CELL PATIENTS. Mediterranean Journal of Hematology and Infectious Diseases, [S. l.], v. 11, n. 1, p. e2019039, 2019. DOI: 10.4084/mjhid.2019.039. Disponível em: https://www.mjhid.org/index.php/mjhid/article/view/2019.039. Acesso em: 13 may. 2021.