Are there clinical phenotypes of homozygous sickle cell disease?
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2004.05025.x/fullpdf
Reference11 articles.
1. Sickle cell anemia with few painful crises is characterized by decreased red cell deformability and increased number of dense cells;Ballas;American Journal of Hematology,1991
2. Estimation of small percentages of foetal haemoglobin;Betke;Nature,1959
3. Chronic leg ulceration in homozygous sickle cell disease: a role of venous incompetence;Clare;British Journal of Haematology,2002
4. Modelling Binary Data
5. Bayesian latent variable models for clustered mixed outcomes;Dunson;Journal of the Royal Statistical Society,2000
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