Observations on two members of the Swedish family with congenital dyserythropoietic anaemia, type III
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1993.tb01923.x/fullpdf
Reference35 articles.
1. Familial erythroid multinuclearity;Wolff;Blood,1951
2. Hereditary benign erythroreticulosis;Bergstrom;Blood,1962
3. Congenital dyserythropoietic anaemia, type III;Goudsmit;Br J Haematol,1972
4. A new case of congenital dyserythropoietic anaemia, type III: studies of the cell cycle distribution and ultrastructure of the erythroblasts and of nucleic acid synthesis in the marrow cells;Wickramasinghe;J Clin Pathol,1982
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1. Mutations in the <i>RACGAP1</i> gene cause autosomal recessive congenital dyserythropoietic anemia type III;Haematologica;2022-10-06
2. Congenital dyserythropoietic anemia types Ib, II, and III: novel variants in the CDIN1 gene and functional study of a novel variant in the KIF23 gene;Annals of Hematology;2020-11-07
3. Congenital dyserythropoietic anemia;International Journal of Hematology;2010-09-07
4. Congenital dyserythropoietic anemia type III with unbalanced globin chain synthesis;European Journal of Haematology;2009-04-24
5. Intravascular haemolysis and increased prevalence of myeloma and monoclonal gammopathy in congenital dyserythropoietic anaemia, type III;European Journal of Haematology;2009-04-24
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