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Hemoglobin
international journal for hemoglobin research
Volume 19, 1995 - Issue 1-2
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Miscellaneous Article

Variant list

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Page 37 | Published online: 07 Jul 2009

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Read on this site (3)

Y. Ohba, Y. Hattori, S. Sakata, Y. Yamashiro, N. Okayama, T. Hirano, T. Nakanishi, A. Miyazaki & A. Shimizu. (1997) HB Niigata [β1(NAl)VALàLEU]: The Fifte Variant with Retention of the Initiator Methionine and Partial Acetylation. Hemoglobin 21:2, pages 179-186.
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L. Pagano, V. Carbone, G. Fioretti, A. Viola, S. Buffardi, V. Ra Metta, S. Desicato, P. Pucci & C. De Rosa. (1997) Compound Heterozygosity for HB Lepore-Boston and HB Neapolis (Dhonburi) [β T126(H4)VALàGLY] in a Patient from Naples, Italy. Hemoglobin 21:1, pages 1-15.
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T. Harano, K. Harano, R. Kawasaki & K. Kawakami. (1996) Hb Toranomon [β112(G14)Cys → Trp]: A New Unstable Electrophoretically Silent Hemoglobin. Hemoglobin 20:4, pages 361-369.
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Articles from other publishers (10)

Dipika Mohanty, Malay B. Mukherjee, Roshan B. Colah, Mahrukh Wadia, Kanjaksha Ghosh, Guru Prasad Chottray, Dipty Jain, Yazdi Italia, Kumar S. Ashokan, Rajni Kaul, Deepak K. Shukla & Vasantha Muthuswamy. (2013) Spectrum of Hemoglobinopathies Among the Primitive Tribes. Asia Pacific Journal of Public Health 27:2, pages NP562-NP571.
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H. Cario. (2004) Childhood polycythemias/erythrocytoses: classification, diagnosis, clinical presentation, and treatment. Annals of Hematology 84:3, pages 137-145.
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John R Petersen, Anthony O Okorodudu, Amin Mohammad & Deborah A Payne. (2003) Capillary electrophoresis and its application in the clinical laboratory. Clinica Chimica Acta 330:1-2, pages 1-30.
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Mitsutoshi Sugano, Hiroya Hidaka, Kazuyoshi Yamauchi, Tetsuo Nakabayashi, Yumiko Higuchi, Kiyotaka Fujita, Nobuo Okumura, Yoshihisa Ushiyama, Minoru Tozuka & Tsutomu Katsuyama. (2000) Analysis of hemoglobin and globin chain variants by a commonly used capillary isoelectric focusing method. Electrophoresis 21:14, pages 3016-3019.
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H. Wajcman, M.O. Préhu, C. Préhu, Y. Blouquit, D. Promé & F. Galactéros. (1998) Hemoglobin Phnom Penh [α117Phe(H1)-Ile-α118Thr(H2)]; evidence for a hotspot for insertion of residues in the third exon of the α1-globin gene. Human Mutation 11:S1, pages S20-S22.
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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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Olga Drakoulakou, Elisavet Papapanagiotou, Afrodite Loutradi-Anagnostou & Manoussos Papadakis. (1997) δ-Thalassemic phenotype due to two “novel” δ-globin gene mutations: CD11[GTC → GGC (A8)-HbA2-pylos] and CD 85 [TTT → TCT (F1)-HbA2-etolia]. Human Mutation 9:4, pages 344-347.
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Bruno Michel Rajko IgićValérie LerayPeter A. DeddishErvin G. Erdös. (1996) Removal of Arg 141 From the α Chain of Human Hemoglobin by Carboxypeptidases N and M . Circulation Research 78:4, pages 635-642.
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Noboru Komiyama, Jeremy Tame & Kiyoshi Nagai. (1996) A Hemoglobin-Based Blood Substitute: Transplanting a Novel Allosteric Effect of Crocodile Hb. Biological Chemistry Hoppe-Seyler 377:9, pages 543-554.
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A. Dumoulin, L. Kiger, R. Jiang, V. Baudin, C. Vasseur, S.G. Sligar, M.C. Marden, J. Pagnier & C. Poyart. (1995) Loss of allosteric behaviour in recombinant hemoglobin α 2 β 2 9 r )F8)His→Ala: Restoration upon addition of strong effectors . FEBS Letters 374:1, pages 39-42.
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