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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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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Coinheritance of a Novel Mutation on the HBA1 Gene: c.187delG (p.W62fsX66) [codon 62 (–G) (α1)] with the α212 Patchwork Allele and Hb S [β6(A3)Glu→Val, GAG>GTG; HBB: c.20A>T]

By Scheps Karen G.   De Paula Silvia M.   Bitsman Alicia R.   Freigeiro Daniel H.   Basack F. Nora   Pennesi Sandra P.   Varela Viviana  

Hemoglobin, Vol. 37, Iss. 5, 2013-10 ,pp. : 492-500

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The Clinical and Laboratory Spectrum of Hb C [β6(A3)Glu→Lys, G AG> A AG] Disease

By Cook Cathleen M.  

Hemoglobin, Vol. 37, Iss. 1, 2013-02 ,pp. : 16-25

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Association in Cis of the Mutations +20 (C>T) in the 5′ Untranslated Region and IVS-II-745 (C>G) on the β-Globin Gene

By Ropero Paloma  

Hemoglobin, Vol. 37, Iss. 2, 2013-04 ,pp. : 112-118

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