Sickle cell?haemoglobin E (HbSE) compound heterozygosity: a clinical and haematological study
Author:
Publisher
Wiley
Subject
Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2257.2006.00886.x/fullpdf
Reference30 articles.
1. The Hemoglobin E Syndromes. II. Sickle-Cell—Hemoglobin E Disease
2. The First Observation of Sickle-Cell Hæmoglobin E Disease
3. Polymorphism and Natural Selection in Human Populations
4. Neonatal screening for haemoglobinopathies: the results of a 10-year programme in an English Health Region
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