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Hemoglobin
international journal for hemoglobin research
Volume 4, 1980 - Issue 3-4
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Original Article

Homozygous Delta Thalassemia in Japan

Y. Ohta First Department of Internal Medicine Faculty of Medicine, Ehime University, Ehime, Japan
,
M. Yasukawa First Department of Internal Medicine Faculty of Medicine, Ehime University, Ehime, Japan
,
S. Saito First Department of Internal Medicine Faculty of Medicine, Ehime University, Ehime, Japan
,
S. Fujita First Department of Internal Medicine Faculty of Medicine, Ehime University, Ehime, Japan
&
Y. Kobayashi First Department of Internal Medicine Faculty of Medicine, Ehime University, Ehime, Japan
Pages 417-425 | Published online: 07 Jul 2009

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Azam Amirian, Masoomeh Jafarinejad, Alireza R. Kordafshari, Marjan Mosayyebzadeh, Morteza Karimipoor & Sirous Zeinali. (2010) Identification of a Novel δ-Globin Gene Mutation in an Iranian Family. Hemoglobin 34:6, pages 594-598.
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T. H. J. Huisman & M. F. H. Carver. (1998) The β-and -Thalassemia Repository (Ninth Edition; Part I). Hemoglobin 22:2, pages 169-195.
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S. Fujita, Y. Ohta, S. Saito, Y. Kobayashi, Y. Naritomi, T. Kawaguchi, T. Imamura, Y. Wada & A. Hayashi. (1985) Hemoglobin A2 Honai (α2δ290(F6)GLU—VAL): A new Delta Chain Variant. Hemoglobin 9:6, pages 597-607.
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Y. Ohba, Y. Hasegawa, H. Amino, S. Miwa, T. Nakatsuji, Y. Hattori & T. Miyaji. (1983) Hemoglobin Saitama Or β117 (G19) His→Pro, A New Variant Causing Hemolytic Disease. Hemoglobin 7:1, pages 47-56.
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Articles from other publishers (8)

Giovanna De Simone, Alberto Quattrocchi, Benedetta Mancini, Alessandra di Masi, Clara Nervi & Paolo Ascenzi. (2022) Thalassemias: from gene to therapy. Molecular Aspects of Medicine 84, pages 101028.
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Abdulrahman Alsultan, Duyen A. Ngo, John J. Farrell, Idowu Akinsheye, Nadia Solovieff, Hazem A. Ghabbour, Amein Al‐Ali, Ahmed Alsuliman, Muneer Al‐Baghshi, Waleed Albu‐Ali, Mohammed Alabdulaali, Clinton T. Baldwin, Lindsay A. Farrer, Hong Luo, Efthymia Melista, Surinder Safaya, Maxwell NwaruJr.Jr., David H.K. Chui & Martin H. Steinberg. (2012) A functional promoter polymorphism of the δ‐globin gene is a specific marker of the Arab‐Indian haplotype. American Journal of Hematology 87:8, pages 824-826.
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Manoussos Papadakis, Elisavet Papapanagiotou & Afrodite Loutradi-Anagnostou. (1997) Scanning method of identify the molecular heterogeneity of δ-globin gene especially in δ-thalassemias: Detection of three novel substitutions in the promoter region of the gene. Human Mutation 9:5, pages 465-472.
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R. Ouazana, D. Bozon, F. Baklouti, C. Gonnet, J. Delaunay & J. Godet. (1989) δ°-Thalassemia in cis of β Knossos -globin gene Normal structure and normal transient expression of the δ-globin gene . FEBS Letters 252:1-2, pages 53-57.
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Shuji Saito. (1984) Study of abnormal hemoglobin in Ehime, Japan: Two structural variants of hemoglobin A (Hb I and Hb J iran) and structural and synthetic variants of delta chain. Japanese Journal of Human Genetics 29:3, pages 335-351.
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M.H. Steinberg & J.G. AdamsIIIIII. (1982) β-Thalassemia-? Selected pseudogenes. Medical Hypotheses 9:6, pages 599-604.
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Martin H. Steinberg & Junius G. Adams. (2006) Thalassemia: Recent insights into molecular mechanisms. American Journal of Hematology 12:1, pages 81-92.
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John T. Wilson, Lois B. Wilson & Yoshiro Ohta. (1981) A case of homozygous δ thalassemia not due to a deletion of the δ globin structural gene. Biochemical and Biophysical Research Communications 99:4, pages 1035-1039.
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