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Hemoglobin|March 17, 2007
Thalassemias and other hemoglobinopathies in the Republic of MacedoniaGeorgi D EfremovHemoglobin|March 17, 2007
Further identification of Hb G-Coushatta [beta22(B4)Glu-->Ala (GAA-->GCA)] in Thailand by the polymerase chain reaction-single-strand conformation polymorphism technique and by amplification refractory mutation system-polymerase chain reactionWorrawut Chinchang, Vip ViprakasitHemoglobin|March 17, 2007
High oxygen affinity hemoglobin variant in a Canadian family: Hb Bunbury [beta94(FG1)Asp-->Asn, GAC-->AAC]Lynda Walker, Barry Eng, Andrew McFarlane, et al.Hemoglobin|January 1, 1991
Monozygotic twins with sickle cell anemia and discordant clinical courses: clinical and laboratory studiesB R Amin, R M Bauersachs, H J Meiselman, et al.Hemoglobin|July 15, 2006
Surface plasmon resonance-based molecular detection of Hb S [beta6(A3)Glu-->Val, GAG-->GTG] at the gene levelErol O Atalay, Emre Ustel, Sanem Yildiz, et al.Hemoglobin|December 10, 2008
Prenatal diagnosis for beta-thalassemia major in the Iranian Province of HormozganPooneh Nikuei, Valeh Hadavi, Minoo Rajaei, et al.Hemoglobin|December 10, 2008
Association of mild and severely unstable alpha chain variants: the first observation of a compound heterozygote with Hb Setif [alpha94(G1)Asp-->Tyr (alpha2)] and Hb Agrinio [alpha29(B10)Leu-->Pro (alpha2)] in a Greek familyVarvara Douna, Ioannis Papassotiriou, Alexandra Stamoulakatou, et al.Hemoglobin|April 18, 2009
Abnormal glucose tolerance in beta-thalassemia: assessment of risk factorsMona Hafez, Ilham Youssry, Fayza Abd El-Hamed, et al.Hemoglobin|April 18, 2009
alpha-Thalassemia mutation analyses in Mazandaran province, North IranAhmad Tamaddoni, Valeh Hadavi, Nima Hafezi Nejad, et al.Hemoglobin|April 18, 2009
Frequency of alpha-globin gene triplications and their interaction with beta-thalassemia mutationsPiero C Giordano, Margaretha Bakker-Verwij, Cornelis L HarteveldPageof 238