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

Informa Healthcare

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Two New δ-Globin Gene Variants: Hb A 2 -Saint-Etienne [δ14(A11)Leu→Pro ( HBD : c.44T>C)] and Hb A 2 -Marseille [δ22(B4) Ala→Lys ( HBD : c.67G>A;68C>A)]

By Joly Philippe  

Hemoglobin, Vol. 37, Iss. 1, 2013-02 ,pp. : 80-84

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Apolipoprotein E Gene Polymorphism in a Chinese Population with Vascular Dementia: A Meta-Analysis

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Dementia and Geriatric Cognitive Disorders, Vol. 33, Iss. 2-3, 2012-03 ,pp. : 96-103

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Identification of the First Mutation in a Bre Motif of the β-Globin Gene and its Inheritance with two Other α-Globin Gene Mutations in a Lebanese Family

By Inati Adlette  

Hemoglobin, Vol. 37, Iss. 2, 2013-04 ,pp. : 171-175

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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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