Congenital Dyserythropoietic Anemia
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Publisher
Springer Nature Singapore
Link
https://link.springer.com/content/pdf/10.1007/978-981-99-8933-1_6
Reference9 articles.
1. Allali S, Brousse V, Sacri AS, et al. Anemia in children: prevalence, causes, diagnostic work-up, and long-term consequences. Expert Rev Hematol. 2017;10:1023–8.
2. Lolascon A, Esposito MR, Russo R. Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach. Haemotologica. 2012;97:178–1794. https://doi.org/10.3324/haematol.2012.072207.
3. Heimpel H, Forteza-Vila J, Queisser W, Spiertz E. Electron and light microscopic study of the erythroblasts of patients with congenital dyserythropoietic anemia. Blood. 1971;37(3):299–310.
4. Crookston JH, Crookston MC, Burnie KL, Francombe WH, Dacie JV, Davis JA, et al. Hereditary erythroblastic multinuclearity associated with a positive acidified-serum test: a type of congenital dyserythropoietic anemia. Br J Haematol. 1969;17(1):11–26.
5. Anselstetter V, Horstmann K, Heimpel H. Congenital dyserythropoietic anaemia, types I and II: aberrant pattern of erythrocyte membrane proteins in CDA II, as revealed by two-dimensional polyacrylamide gel electrophoresis. Br J Haematol. 1977;35(2):209–15.
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