A 13-bp Deletion in the 3′ Untranslated Region of the β-Globin Gene Causes β-Thalassemia Major in Compound Heterozygosity with IVSII-1 Mutation

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Medical Principles and Practice, Vol. 20, Iss. 5, 2011-07 ,pp. : 488-490

Karger

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Mild β + -Thalassemia Associated With Two Linked Sequence Variants: IVS-II-839 (T>C) and IVS-II-844 (C>A)

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

Hemoglobin, Vol. 37, Iss. 4, 2013-08 ,pp. : 378-386

Informa Healthcare

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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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Homozygosity for the Severe β + -Thalassemia Mutation [IVS-I-5 (G>C)] Causes the Phenotype of Thalassemia Trait: An Extremely Rare Presentation

By Bohara Vinaykumar   Raut Lalit   Badarkhe Girish   Roy Siddartha S.   Chaudhuri Utpal  

Hemoglobin, Vol. 37, Iss. 1, 2013-02 ,pp. : 101-105

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Identification of Two Rare β-Globin Gene Mutations in a Patient with β-Thalassemia Intermedia from Azerbaijan

By Asadov Chingiz D.  

Hemoglobin, Vol. 37, Iss. 3, 2013-06 ,pp. : 291-296

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