Detection of Hb Constant Spring [ α 142, Term→Gln, T AA> C AA ( α 2)] in Heterozygotes Combined With β-Thalassemia

By Li You-Qiong  

Hemoglobin, Vol. 37, Iss. 2, 2013-04 ,pp. : 197-200

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Hb Plasencia [ α 125(H8)Leu→Arg ( α 2)] is a Frequent Cause of α + -Thalassemia in the Portuguese Population

By Cunha Elizabete  

Hemoglobin, Vol. 37, Iss. 2, 2013-04 ,pp. : 183-187

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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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Association of Hb Thailand [ α 56(E5)Lys→Thr] and Hb Phnom Penh [ α 117(GH5)-Ile- α 118(H1)] with α 0 -Thalassemia: Molecular and Hematological Features and Differential Diagnosis

By Singha Kritsada  

Hemoglobin, Vol. 37, Iss. 1, 2013-02 ,pp. : 37-47

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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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