The Different Types of α-Thalassemia-2: Genetic Aspects
Author:
Publisher
Informa UK Limited
Subject
Biochemistry (medical),Clinical Biochemistry,Genetics (clinical),Hematology
Link
http://www.tandfonline.com/doi/pdf/10.3109/03630268808991633
Reference28 articles.
1. New Hemoglobin Possessing a Higher Electrophoretic Mobility than Normal Adult Hemoglobin
2. IS THE HUMAN GLOBIN α-CHAIN LOCUS DUPLICATED?
3. Gene deletion as the cause of α thalassaemia: Genetic lesion in homozygous α thalassaemia (hydrops fetalis)
4. Gene deletion as the cause of α thalassaemia: The severe form of α thalassaemia is caused by a haemoglobin gene deletion
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2. Is Hb A2Elevated in Adults with Sickle-A-Thalassemi (βS/βS; -α/-α);Hemoglobin;1997-01
3. Detection of common deletional α-thalassemia-2 determinants by PCR;American Journal of Hematology;1994-07
4. Prenatal diagnosis of unusual hemoglobinopathies;American Journal of Medical Genetics;1994-03-01
5. MOLECULAR SCREENING FOR HAEMOGLOBIN CONSTANT SPRING;The Lancet;1989-05
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