A heterozygote for HbβS, HbβC and HbαG Philadelphia in a family presenting evidence for heterogeneity of hemoglobin alpha chain loci
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference41 articles.
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4. Another family showing the interaction of the genes for Hb G and Hb S;Lie-Injo;Acta Haematol,1968
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1. Sickle cell haemoglobin and its interactions with other variant haemoglobins and with thalassaemias;Haemoglobinopathy Diagnosis;2020-02-28
2. Molecular Interactions Between Hb α-G Philadelphia, HbC, and HbS: Phenotypic Implications for SC α-G Philadelphia Disease;Blood;1997-10-01
3. Molecular Interactions Between Hb α-G Philadelphia, HbC, and HbS: Phenotypic Implications for SC α-G Philadelphia Disease;Blood;1997-10-01
4. Case Report: Alpha G-Philadelphia, Beta O-Arab, and Beta C Globins Present in a Single Patient;The American Journal of the Medical Sciences;1993-05
5. Usefulness of HPLC Methodology for the Characterization of Combinations of the Common β Chain Variants HBS S, C, and O-ARAB, and the α Chain Variant HB G-Philadelphia;Hemoglobin;1993-01
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