A novel case of haemoglobin H disease associated with clinical and morphological characteristics of congenital dyserythropoietic anaemia type I
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1600-0609.2002.01590.x/fullpdf
Reference15 articles.
1. A review of the molecular genetics of the human α-globin gene cluster;Higgs;Blood,1989
2. Congenital dyserythropoietic anemias;Wickramasinghe;Curr Opin Hematol,2000
3. Dyserythropoiesis and congenital dyserythropoietic anaemias;Wickramasinghe;Br J Haematol,1997
4. Electron and light microscopic study of the erythroblasts of patients with congenital dyserythropoietic anemia;Heimpel;Blood,1971
5. Alterations of globin chain synthesis and of red cell membrane proteins in congenital dyserythropoietic anemia I and II;Alloisio;Pediatr Res,1982
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1. A case of congenital dyserythropoietic anemia masked by hemoglobin H disease;Mediterranean Journal of Hematology and Infectious Diseases;2024-06-29
2. Non-deletional haemoglobin H (Hb H) disease morphologically masquerading as congenital dyserythropoietic anaemia type II: a diagnostic pitfall;Journal of Clinical Pathology;2023-12-20
3. The Congenital Dyserythropoietic Anemias;Hematology/Oncology Clinics of North America;2009-04
4. Advances in the understanding of the congenital dyserythropoietic anaemias;British Journal of Haematology;2005-11
5. Defective organization of the erythroid cell membrane in a novel case of congenital anemia;Blood Cells, Molecules, and Diseases;2003-01
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