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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Silent β-Thalassemia Mutations at −101 (C>T) and −71 (C>T) and Their Coinheritance with the Sickle Cell Mutation in Bahrain

By Al Moamen Nabeel J.  

Hemoglobin, Vol. 37, Iss. 4, 2013-08 ,pp. : 369-377

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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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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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Hb Grove City [β38(C4)Thr→Ser, A C C>A G C; HBB : c.116C>G]: A New Low Oxygen Affinity β Chain Variant

By Taliercio Rachel M.  

Hemoglobin, Vol. 37, Iss. 4, 2013-08 ,pp. : 396-403

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