Hb AHVAZ [α83(F4)Leu→Arg, CTG>CGG (α2); HBA2: c.251T>G],A New Hemoglobin Variant of the α2-Globin Gene

By Hamid Mohammad   Shariati Gholamreza   Saberi Alihossein   Galehdari Hamid   Kaikhaei Bijan   Mohammadi-Anaei Marziye  

Hemoglobin, Vol. 37, Iss. 5, 2013-10 ,pp. : 477-480

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Coinheritance of a Novel Mutation on the HBA1 Gene: c.187delG (p.W62fsX66) [codon 62 (–G) (α1)] with the α212 Patchwork Allele and Hb S [β6(A3)Glu→Val, GAG>GTG; HBB: c.20A>T]

By Scheps Karen G.   De Paula Silvia M.   Bitsman Alicia R.   Freigeiro Daniel H.   Basack F. Nora   Pennesi Sandra P.   Varela Viviana  

Hemoglobin, Vol. 37, Iss. 5, 2013-10 ,pp. : 492-500

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Hb Fulton-Georgia [α20(B1)His→Pro; HBA1: c.62A>C]: A New α-Globin Variant Coinherited with α-Thalassemia-2 (3.7 kb deletion) and Hb SC Disease

By Zhuang Lina   Patel Niren   Bryant Shanequa   Kutlar Abdullah   Kutlar Ferdane   Young Andrew N.  

Hemoglobin, Vol. 37, Iss. 5, 2013-10 ,pp. : 481-485

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Towards worldwide standardisation of HbA₁c determination

By Miedema K.  

Diabetologia, Vol. 47, Iss. 7, 2004-07 ,pp. : 1143-1148

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Interaction of Hb Adana ( HBA2 : c.179G>A) with Deletional and Nondeletional α + -Thalassemia Mutations: Diverse Hematological and Clinical Features

By Nainggolan Ita M.  

Hemoglobin, Vol. 37, Iss. 3, 2013-06 ,pp. : 297-305

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