Association between sickle cell anemia and alpha thalassemia reveals a high prevalence of the α(3.7) triplication in congolese patients than in worldwide series

Documenti analoghi

• Protective BCL11A and HBS1L‐MYB polymorphisms in a cohort of 102 Congolese patients suffering from sickle cell anemia
  di: Mikobi, Tite Minga, et al.
  Pubblicazione: (2017)
• Correlation between the Lactate Dehydrogenase Levels with Laboratory Variables in the Clinical Severity of Sickle Cell Anemia in Congolese Patients
  di: Mikobi, Tite Minga, et al.
  Pubblicazione: (2015)
• Clinical phenotypes and the biological parameters of Congolese patients suffering from sickle cell anemia: A first report from Central Africa
  di: Mikobi, Tite M., et al.
  Pubblicazione: (2017)
• Homozygous Deletion Alpha-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 the Democratic Republic of Congo
  di: Mikobi, Tite Minga, et al.
  Pubblicazione: (2019)
• Meningocele in a Congolese Female with Beckwith-Wiedemann Phenotype
  di: Mbuyi-Musanzayi, Sébastien, et al.
  Pubblicazione: (2014)