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Hemoglobin
international journal for hemoglobin research
Volume 1, 1976 - Issue 2
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Original Article

Another Form of tie Hereditary Persistence of Fetal Hemoglobin (The Atlanta Type)?

C. Altay Laboratory of Protein Chemistry, Department of Cell and Molecular Biology and Comprehensive Sickle Cell Center, Medical College of Georgia and Veterans Administration Hospital, Augusta, Georgia, 30902, USA; Division of Chemistry and Chemical Engineering (Contribution No. 5394), California Institute of Technology, Pasadena, California, 91125, USA
,
T. H. J. Huisman Laboratory of Protein Chemistry, Department of Cell and Molecular Biology and Comprehensive Sickle Cell Center, Medical College of Georgia and Veterans Administration Hospital, Augusta, Georgia, 30902, USA; Division of Chemistry and Chemical Engineering (Contribution No. 5394), California Institute of Technology, Pasadena, California, 91125, USA
&
W. A. Schroeder Laboratory of Protein Chemistry, Department of Cell and Molecular Biology and Comprehensive Sickle Cell Center, Medical College of Georgia and Veterans Administration Hospital, Augusta, Georgia, 30902, USA; Division of Chemistry and Chemical Engineering (Contribution No. 5394), California Institute of Technology, Pasadena, California, 91125, USA
Pages 125-133 | Published online: 07 Jul 2009

Citations (19)

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Read on this site (2)

Georgi D. Efremov. (2001) FORTY-FOUR YEARS (1955–1999) DEVOTED TO HEMOGLOBIN RESEARCH: TITUS H. J. HUISMAN (1923–1999). Hemoglobin 25:2, pages 125-168.
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T. H. J. Huisman, S. S. Chen, T. Nakatsuji & F. Kutlar. (1985) A second Family with the Atlanta type of HPFH. Hemoglobin 9:4, pages 393-398.
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Articles from other publishers (17)

Swee Lay Thein & Stephan Menzel. (2009) Discovering the genetics underlying foetal haemoglobin production in adults. British Journal of Haematology 145:4, pages 455-467.
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D.J. Weatherall & J.B. Clegg. 2001. The Thalassaemia Syndromes. The Thalassaemia Syndromes 733 821 .
T.H.J. Huisman. (1997) Gamma chain abnormal human fetal hemoglobin variants. American Journal of Hematology 55:3, pages 159-163.
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J. Rochette, J.E. Craig, S.L. Thein & J. Rochette. (1994) Fetal hemoglobin levels in adults. Blood Reviews 8:4, pages 213-224.
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A. J. Dimovski, D. G. Efremov, L‐H. Gu & T. H. J. Huisman. (2008) The relative levels of β A and β S mRNAs in Hb S heterozygotes and in patients with Hb S‐β + ‐thalassaemia or Hb S‐β + ‐HPFH combinations . British Journal of Haematology 87:2, pages 353-356.
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G. Przybylski, H. Oettle, W. D. Ludwig, W. Siegert & C. A. Schmidt. (2008) Molecular characterization of illegitimate TCRδ gene rearrangements in acute myeloid leukaemia. British Journal of Haematology 87:2, pages 301-307.
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William G. Wood. (1993) 7 Increased HbF in adult life. Baillière's Clinical Haematology 6:1, pages 177-213.
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Jacques A. Bollekens & Bernard G. Forget. (1991) δβ Thalassemia and Hereditary Persistence of Fetal Hemoglobin. Hematology/Oncology Clinics of North America 5:3, pages 399-422.
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H. J. Huang, T. A. Stoming, H. F. Harris, F. Kutlar & T. H. J. Huisman. (2006) The greek a γβ + ‐hpfh observed in a large black family . American Journal of Hematology 25:4, pages 401-408.
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G. D. Efremov, V. Filifcče, I. Gjorgovski, D. Juričič, N. Stojanovski, T. Harano, T. Nakatsuji, A. Kutlar, F. Kutlar, I. Bakioglu & T. H. J. Huisman. (2008) G γ A γ(δβ)°‐thalassaemia and a new form of γ globin gene triplication identified in the Yugoslavian population . British Journal of Haematology 63:1, pages 17-28.
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J. G. GILMAN, T. HARANO, T. NAKATSUJI, I. BAKIOGLU, A. L. REESE, M. B. GARDINER & T. H. J. HUISMAN. (1985) The Ratio of the G ? and A ? Chains: Variations due to Anomalies at the Molecular Level . Annals of the New York Academy of Sciences 445:1 Fifth Cooley', pages 235-247.
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Josef Prchal, G. Stamatoyannopoulos & John M. Opitz. (2005) Two siblings with unusually mild homozygous β‐thalassemia: A didactic example of the effect of a nonallelic modifier gene on the expressivity of a monogenic disorder. American Journal of Medical Genetics 10:3, pages 291-300.
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W. A. Schroeder & T. H. J. Huisman. (1980) HEMOGLOBIN F IN ? THALASSEMIA AND RELATED CONDITIONS. Annals of the New York Academy of Sciences 344:1 Fourth Cooley, pages 240-252.
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W. G. Wood, J. B. Clegg & D. J. Weatherall. (2008) HEREDITARY PERSISTENCE OF FETAL HAEMOGLOBIN (HPFH) AND δβ THALASSAEMIA. British Journal of Haematology 43:4, pages 509-520.
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D R Higgs, J B Clegg, W G Wood & D J Weatherall. (1979) G gamma beta + type of hereditary persistence of fetal haemoglobin in association with Hb C.. Journal of Medical Genetics 16:4, pages 288-295.
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Titus H. J. Huisman. (2006) Sickle cell anemia as a syndrome: A review of diagnostic features. American Journal of Hematology 6:2, pages 173-184.
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C. Altay, W.A. Schroeder & T.H.J. Huisman. (2013) The G γ‐δβ‐thalassemia and G γ‐β°‐HPFH conditions in combination with β‐thalassemia and Hb S . American Journal of Hematology 3:1, pages 1-14.
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