Co-inheritance of Hb Pak Num Po, a novel ?1 gene mutation, and ?0 thalassemia associated with transfusion-dependent Hb H disease-Reference-Cited by-同舟云学术

Co-inheritance of Hb Pak Num Po, a novel ?1 gene mutation, and ?0 thalassemia associated with transfusion-dependent Hb H disease

Published:2004 Issue:3 Volume:75 Page:157-163
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Viprakasit Vip,Tanphaichitr Voravarn S.,Veerakul Gavivann,Chinchang Worrawut,Petrarat Siripan,Pung-Amritt Parichat,Higgs Douglas R.

Publisher

Wiley

Subject

Hematology

Reference14 articles.

1. Clinical and laboratory features of the ? thalassemia syndrome. In: et al., editors. Disorders of hemoglobin. Cambridge: Cambridge University Press; 2001. p 431-469.

2. Genetic and Clinical Features of Hemoglobin H Disease in Chinese Patients

3. Molecular mechanisms of ? thalassemia. In: et al., editors. Disorders of hemoglobin. Cambridge: Cambridge University Press; 2001. p 405-430.

4. Molecular defects in Hb H hydrops fetalis

5. Hb H hydrops foetalis syndrome: a case report and review of literature

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