Utility and Importance of Accurate Hb A₂ Measurements for Defining a Strategy for β-Thalassemia Screening: Experience in the Balearic Islands, Spain

By López-Escribano Herminio   Parera Maria M.   Guix Pilar   Castro José A.   Ramon Misericòrdia   Picornell Antònia  

Hemoglobin, Vol. 37, Iss. 6, 2013-12 ,pp. : 593-598

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Thalassemia and Premarital Screening: Potential for Implementation of a Screening Program Among Young People in Pakistan

By Mirza Arslan  

Hemoglobin, Vol. 37, Iss. 2, 2013-04 ,pp. : 160-170

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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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Normal Hb A 2 β-Thalassemia Trait: Frameshift Mutation ( HBB : c.187_251dup) in Cis with the Hb A 2' δ-Globin Gene Missense Mutation ( HBD : c.49G>C)

By Waye John S.   Eng Barry   Hellens Laurie   Hohenadel Betty-Ann   Nakamura Lisa M.   Walker Lynda  

Hemoglobin, Vol. 37, Iss. 2, 2013-04 ,pp. : 201-204

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Erythrocytosis in a Child due to Hb Andrew-Minneapolis [β144(HC1)Lys→Asn (AA G >AA T or AA C )] Associated with a Spanish (δβ) 0 -Thalassemia

By Ropero Paloma  

Hemoglobin, Vol. 37, Iss. 1, 2013-02 ,pp. : 48-55

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