A combination of the -α(3.7) and --(MEDII) alleles causing hemoglobin H disease in a Brazilian patient

Lignende værker

• A combination of the -α3.7 and --MEDII alleles causing hemoglobin H disease in a Brazilian patient
  af: Roberta Dorta Ferreira, et al.
• Rare α(0)-thalassemia deletions detected by MLPA in five unrelated Brazilian patients
  af: Mota, Natália O., et al.
  Udgivet: (2017)
• α-chain hemoglobin variants with electrophoretic mobility similar to that of hemoglobin S in newborn screening programs
  af: Sonati, Maria de Fátima
  Udgivet: (2013)
• Hb H disease resulting from the association of an α(0)-thalassemia allele [-(α)(20.5)] with an unstable α-globin variant [Hb Icaria]: First report on the occurrence in Brazil
  af: Kimura, Elza M., et al.
  Udgivet: (2009)
• Prevalence of α-thalassemia 3.7 kb deletion in the adult population of Rio Grande do Norte, Brazil
  af: de Medeiros Alcoforado, Gustavo Henrique, et al.
  Udgivet: (2012)