Occurrence ofGγ Hb F in Greek HPFH: Analysis of Heterozygotes and Compound Heterozygotes with β Thalassaemia
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1979.tb03785.x/fullpdf
Reference38 articles.
1. A Comparison of the Homozygous States forGγ andGγAγ δβ Thalassaemia
2. Abnormal human haemoglobins
3. Hereditary Persistence of Fetal Hemoglobin: A Study of 79 Affected Persons in 15 Negro Families in Baltimore
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1. Restriction endonuclease maps of the β-like globin gene cluster in the British and Greek forms of HPFH, and for one example of Gγβ+ HPFH;British Journal of Haematology;2008-07-07
2. A 12-year preventive program for β-thalassemia in Northern Sardinia;Clinical Genetics;2008-06-28
3. Fetal hemoglobin expression in the compound heterozygous state for ?117 (G?A)A? HPFH and IVSII-745 (C?G) ?+ thalassemia: A case study;American Journal of Hematology;1999-06
4. Fetal hemoglobin expression in compound heterozygotes for −117 (G→A)Aγ HPFH and β039 nonsense thalassemia;American Journal of Hematology;1995-08
5. A genetic marker for elevated levels of haemoglobin F in homozygous sickle cell disease?;British Journal of Haematology;1985-06
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