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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Prevalence and Molecular Characterization of β-Thalassemia in the State of Bahia, Brazil: First Identification of Mutation HBB : c.135delC in Brazil

By Fonseca Silvana F.  

Hemoglobin, Vol. 37, Iss. 3, 2013-06 ,pp. : 285-290

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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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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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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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