Hemoglobinopathies mimicking Hb S/β-thalassemia: Hb S/S with α-thalassemia and Hb S/Volga

Author:

Luo Hong-Yuan,Heeney Matthew,Wang Winfred C.,Eung Shawn H.,Ware Russell E.,Steinberg Martin H.,Chui David H.K.

Publisher

Wiley

Subject

Hematology

Reference26 articles.

1. Alpha-thalassemia in blacks: genetic and clinical aspects and interactions with the sickle hemoglobin gene

2. Universal Newborn Screening for Hb H Disease in California

3. Molecular mechanisms of β thalassemia. In: , , , editors. Disorders of hemoglobin genetics, pathophysiology, and clinical management. Cambridge: Cambridge University Press; 2001. p 252–276.

4. Compound heterozygous and other hemoglobinopathies. In: , , , editors. Disorders of hemoglobin: genetics, pathophysiology, and clinical management. Cambridge: Cambridge University Press; 2001. p 786–810.

5. Severe hemolytic anemia associated with Hb Volga [β27(B9)Ala→Asp]: GCC→GAC at codon 27 in a Turkish family

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