Detection of Hb H Disease Genotypes Common in Northern Thailand by Quantitative Real-Time Polymerase Chain Reaction and High Resolution Melting Analyses

By Seeratanachot Teerapat   Sanguansermsri Torpong   Shimbhu Dawan  

Hemoglobin, Vol. 37, Iss. 6, 2013-12 ,pp. : 574-583

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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 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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CODON 30 (–GAG) (α2): Hematological Parameters in Heterozygotes and also Patients with Hb H Disease

By Yang Yu   Li Dong-Zhi  

Hemoglobin, Vol. 37, Iss. 6, 2013-12 ,pp. : 599-603

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Variable Presentation of HB H Disease Due to Homozygosity for the Rare Polyadenylation Signal A T Indian (AATA AA >AATA- -) Mutation in Four Indian Families

By Nair Sona B.   Nadkarni Anita H.   Ghosh Kanjaksha   Colah Roshan B.  

Hemoglobin, Vol. 37, Iss. 3, 2013-06 ,pp. : 277-284

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