An Individual with Hb-Lepore-Baltimore- δβ-Thalassaemia in a Yugoslavian Family
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.1976.tb01122.x/fullpdf
Reference33 articles.
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2. Protein coagulation and its reversal. The preparation of insoluble globin and soluble globin;Anson;J Gen Physiol,1930
3. Estimation of small percentages of foetal haemoglobin;Betke;Nature,1959
4. Homozygous βδ thalassaemia (βδ microcythaemia);Brancati;Nature,1966
5. Separation of the α- and β-chains of human haemoglobin;Clegg;J Mol Biol,1966
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2. Fetal hemoglobin elevation in Hb lepore heterozygotes and its correlation with β globin cluster linked determinants;American Journal of Hematology;2002-01-18
3. FORTY-FOUR YEARS (1955–1999) DEVOTED TO HEMOGLOBIN RESEARCH: TITUS H. J. HUISMAN (1923–1999);Hemoglobin;2001-01
4. Special Feature Hemoglobinopathies in Yugoslavia: an Update;Hemoglobin;1992-01
5. Hb Lepore-Baltimore in a North Sardinian Family;Hemoglobin;1990-01
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