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Hemoglobin
international journal for hemoglobin research
Volume 2, 1978 - Issue 2
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Original Article

Biosynthetic Ratio of Labelled Globin Chains in Human Reticulocytes, Determined by Electrophoresis on Cellulose Acetate

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Pages 129-141 | Received 20 Apr 1977, Accepted 13 Feb 1978, Published online: 07 Jul 2009

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Read on this site (5)

R. Galanello, S. Satta, M. G. Pirroni, M. Travi & L. Maccioni. (1998) Globin Chain Synthesis Analysis by High Performance Liquid Chroniatography in the Screening of Thalassemia Syndromes. Hemoglobin 22:5-6, pages 501-508.
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S. Rahbar & Y. Asmerom. (1989) Rapid HPLC Techniques for Globin Chain Synthesis Studies. Hemoglobin 13:5, pages 475-487.
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J. Bardakdjian, N. Arous, J. Kister, Y. Blouquit, Th. Giacomini, C. Lacombe, J. Riou, R. Hafsia, J. Rosa & F. Galacteros. (1987) Further Characterization of Hb Henri Mondor or α2β226(B8)Glu→Val. Hemoglobin 11:1, pages 1-11.
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J. Delanoe-Garin, N. Arous, Y. Blouquit, R. Hafsia, J. Bardakdjian, C. Lacombe, J. Rosa & F. Galacteros. (1985) Hemoglobin Kenitra α2β269 (E13) Gly→Arg. A new β Variant of Elevated Expression Associated with α-Thalassemia, Found in a Moroccan Woman. Hemoglobin 9:1, pages 1-9.
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. (1980) Short Communications. Hemoglobin 4:2, pages 195-200.
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Articles from other publishers (11)

Cedric H. L. Shackleton & H. Ewa Witkowska. 1994. Mass Spectrometry. Mass Spectrometry 135 199 .
J. Bardakdjian‐Michau, J. Delanoe‐Garin, C. Lacombe, Y. Blouquit, J. Riou, F. Galacteros, S. Fucharoen, P. Winichagoon, P. Wasi & J. Kister. (2006) Hemoglobin dhonburi α 2 β 2 126 (H4) Val → Gly: A new unstable β variant producing a β‐thalassemia intermedia phenotype in association with β°‐Thalassemia . American Journal of Hematology 35:2, pages 96-99.
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P. Basset, F. Braconnier & J. Rosa. (1982) An update on electrophoretic and chromatographic methods in the diagnosis of hemoglobinopathies. Journal of Chromatography B: Biomedical Sciences and Applications 227:2, pages 267-304.
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M. Boccacci, A. Massa & L. Tentori. (1981) Application of cellulose acetate electrophoresis to globin chain separation for antenatal diagnosis of beta thalassemia. Clinica Chimica Acta 116:2, pages 137-142.
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M. Oort, W. Heerspink, D. Roos, R. A. Flavell & L. F. Bernini. (1981) Haemolytic Disease of the Newborn and Chronic Anaemia Induced by γ β Thalassaemia in a Dutch Family. British Journal of Haematology 48:2, pages 251-262.
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M. Oort, W. Heerspink, D. Roos, R. A. Flavell & L. F. Bernini. (2008) Haemolytic Disease of the Newborn and Chronic Anaemia Induced by γβ Thalassaemia in a Dutch Family. British Journal of Haematology 48:2, pages 251-262.
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Mario Furbetta, Antonella Angius, Ada Ximenes, Cristina Rosatelli, M. Teresa Scalas, Teresa Tuveri, Angela M. Falchi & Antonio Cao. (2008) DIFFICULTIES IN ANTENATAL DIAGNOSIS OF INHERITED HAEMOGLOBINOPATHIES: γ‐CHAIN VARIANTS. British Journal of Haematology 47:2, pages 319-321.
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Luciano Vettore, Maria Concetta De Matteis & Patrizia Zampini. (2006) A new density gradient system for the separation of human red blood cells. American Journal of Hematology 8:3, pages 291-297.
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L. H. T. Van der Ploeg, A. Konings, M. Oort, D. Roos, L. Bernini & R. A. Flavell. (1980) γ-β-Thalassaemia studies showing that deletion of the γ- and δ-genes influences β-globin gene expression in man. Nature 283:5748, pages 637-642.
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R. E. GALE, J. B. CLEGG & E. R. HUEHNS. (1979) Human embryonic haemoglobins Gower 1 and Gower 2. Nature 280:5718, pages 162-164.
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A. E. Felice, B. Webber, A. Miller, S. M. Mayson, H. F. Harris, J. B. Henson, M. E. Gravely & T. H. J. Huisman. (2006) The association of sickle cell anemia with heterozygous and homozygous α‐thalassemia‐2: In vitro HB chain synthesis. American Journal of Hematology 6:2, pages 91-106.
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