Functional characterization of compound heterozygosity Hb S/Hb Deer Lodge in Brazil by Marcondes J. Sobreira, Thais H. Batista, Rodrigo M. Santana, Gabriela S. Arcanjo, Susan E. Jorge, Magnun N. Santos, Dulcinéia M. Albuquerque, Betânia L. Hatzlhofer, Ana C. dos Anjos, Fernando F. Costa, Aderson S. Araujo, Maria F. Sonati, Antonio R. Lucena-Araujo, Marcos A. Bezerra

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Hb H disease associated with compound heterozygosity for --SEA deletion and a novel alpha globin chain variant (HBA2:c.175C>A) on the distal histidine in a Chinese family by Manna Sun, Jiwu Lou, Wang Xinghe, Ying Zhao, Yunshi Dai, Shuangai Liu, Tizhen Yan

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Clinical and laboratory features of Hemoglobin La Desirade variant in association with sickle cell and alpha thalassemia genes by Salam Alkindi, Shoaib Al Zadjali, Mohamed Al Rawahi, Hamoud Al Haddabi, Shahina Daar, Refaat Abdullah Elsadek, Bahaa Eldeen Diab Sherkawy, Anil Pathare

Subjects: “…Sickle cell trait, sickle cell disease, Hemoglobin La Desirade, unstable hemoglobin variant, alpha thalassemia…”
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Interactions of electrophoretically silent hemoglobin Hekinan II [HBA1:c.84G>T] with various forms of α-thalassemias and other hemoglobinopathies: novel insights into the molecular... by Sitthichai Panyasai, Prasert Chantanaskulwong, Nopphadol Permsripong, Thippawal Mokmued

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Haemoglobin types and variant interference with HbA1c and its association with uncontrolled HbA1c in type 2 diabetes mellitus by Joseph Malaba, Paul Kosiyo, Bernard Guyah

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