Haemoglobin Nicosia. AN α-CHAIN VARIANT AND ITS COMBINATION WITH β-THALASSAEMIA
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1965.tb06592.x/fullpdf
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1. Brief Note: A Variety of Human Hemoglobin with 4 Distinct Electrophoretic Components
2. Alteration in the α-Chain of Hæmoglobin LF rrara
3. The First Observation of an Abnormal Haemoglobin in a Jewish Family: Haemoglobin Beilinson
4. TRIS Buffer for the Demonstration of Haemoglobin A2 by Paper Electrophoresis
5. Ph. Fessas, H. Lehmann, and K. Betke (1962 ). Haemoglobin H and Bart's . : Haemoglobin Colloquium, Wien, 1961, p.74 . Thieme, Stuttgart.
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2. Haemoglobin Inkster (α285aspartic acid → valineβ2) Coexisting with β-Thalassaemia in a Caucasian Family;British Journal of Haematology;1974-03
3. Interaction entre les hémoglobines Stanleyville II et S dans une famille du Zaïre. Etude de l'hybride Stanleyville II/S (α278 lys β26 val);Biochimie;1973-11
4. Is Haemoglobin Gα Philadelphia Linked to α-Thalassaemia?;Acta Haematologica;1971
5. Hemoglobin Hasharon (α247 his(CD5)β2): a hemoglobin found in low concentration;Journal of Clinical Investigation;1969-05-01
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