Type I Congenital Dyserythropoietic Anaemia with Myelopoietic Abnormalities and Hand Malformations
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1978.tb02496.x/fullpdf
Reference25 articles.
1. An immunoradiometric assay for ferritin in the serum of normal subjects and patients with iron deficiency and overload;Addison;J Clin Pathol,1972
2. Congenital dyserythropoietic anaemia, types I and II: aberrant pattern of erythrocyte membrane proteins in CDA II, as revealed by two-dimensional polyacrylamide gel electrophoresis;Anselstetter;Br J Haematol,1977
3. Hereditary benign erythroreticulosis;Bergström;Blood,1962
4. Letter to the Editor;Bethlenfalvay;Blood,1974
5. Congenital dyserythropoietic anemia, type I;Castro;Arch Intern Med,1974
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2. Congenital dyserythropoietic anaemia (CDA) with intrauterine symptoms and early lethal outcome;European Journal of Haematology;2009-04-24
3. Fanconi's Anaemia. Simultaneous onset in 2 Siblings and unusual Cytological Findings;Scandinavian Journal of Haematology;2009-04-24
4. The Congenital Dyserythropoietic Anemias;Hematology/Oncology Clinics of North America;2009-04
5. Congenital dyserythropoietic anemia type I with bone abnormalities, mutations of the CDAN I gene, and significant responsiveness to alpha-interferon therapy;Annals of Hematology;2006-06-10
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