The Genetics and Molecular Basis of Alpha Thalassaemia in Association with Hb S in Jamaican Negroes
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1981.tb02760.x/fullpdf
Reference35 articles.
1. Hemoglobin α Chain Deficiency in Black Children with Variable Quantities of Hemoglobin Bart's at Birth
2. THE FUSION OF TWO PEPTIDE CHAINS IN HEMOGLOBIN LEPORE AND ITS INTERPRETATION AS A GENETIC DELETION
3. Estimation of Small Percentages of Fœtal Hæmoglobin
4. Sickle cell anemia and trait in Southern India: Further studies
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