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Hemoglobin
international journal for hemoglobin research
Volume 10, 1986 - Issue 1
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Original Article

The Identification of Five Rare β-Chain Abnormal Hemoglobins by High Performance Liquid Chromatographic Procedures

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Pages 49-63 | Received 06 Sep 1985, Accepted 05 Nov 1985, Published online: 07 Jul 2009

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Read on this site (6)

A. Yalçin, F. Avcu, C. Beyan, A. Gürgey & A. U. Ural. (1994) A case of HB J-Meerut (or HB J-Birmingham) [α120(H3)ALA→GLU]. Hemoglobin 18:6, pages 433-435.
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M. De Angioletti, G. Maglione, P. Ferranti, C. de Bonis, G. Lacerra, A. Scarallo, L. Pagano, G. Fioretti, R. Cutolo, A. Malorni, P. Pucci & C. Carestia. (1992) HB City of Hope [β69(E13)GLY→SER] in Italy: Association of the Gene with Haplotype IX. Hemoglobin 16:1-2, pages 27-34.
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A. Kutlar, F. Kutlar, M. Aksoy, A. Gurgey, Ç. Altay, J. B. Wilson, J. C. Diaz-Chico, H. Hu & T. H. J. Huisman. (1989) β-Thalassemia Intermedia in Two Turkish Families is Caused by the Interaction of HB Knossos [β27(B9)ALA→SER] and of HB City of hope [β69(E13)Gly→Ser] with B°-Thalassemia. Hemoglobin 13:1, pages 7-16.
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A. Kutlar, F. Kutlar, J. B. Wilson, B. B. Webber, H. Hu & T. H. J. Huisman. (1988) HB F-Austell or α2Gγ240(c6)ARG→LYS. Hemoglobin 12:4, pages 409-411.
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L. Manca, M. Formato, B. Masaia, D. Gallisai & M. Orzalesi. (1987) Hemoglobin Hamilton [β11(A8)VAL →] in Sardinia. Hemoglobin 11:2, pages 161-167.
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Articles from other publishers (5)

Lori D. RacsaHung S. LuuJason Y. ParkMidori MituiCharles F. Timmons. (2014) β-Globin Gene Sequencing of Hemoglobin Austin Revises the Historically Reported Electrophoretic Migration Pattern. Archives of Pathology & Laboratory Medicine 138:6, pages 819-822.
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Yin Wu, Gautam V. Ramani, Qiwei Gai, Latrina C. Lemon & Maria R. Baer. (2010) Rare hemoglobinopathy presenting as progressive dyspnea. American Journal of Hematology 85:5, pages 355-357.
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A. Villegas, J. J. Malcorra, I. Balda, F. Calero, A. Porres, J. L. Alvarez-Sala, D. Espinós, John M. Opitz & James F. Reynolds. (1989) A new Spanish family with Hb Louisville. American Journal of Medical Genetics 32:1, pages 9-14.
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V.B. Jogessar, K. Westermeyer, B.B. Webber, J.B. Wilson, H. Hu, J.M. Gonzalez-Redondo, A. Kutlar & T.H.J. Huisman. (1988) Hb Natal or α2(minus Tyr-Arg)β2: A high oxygen affinity α chain variant with a deleted carboxy-terminus resulting from a TAC → TAA (Tyr → terminating codon) mutation in codon α140. Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression 951:1, pages 36-41.
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Y. Hattori, F. Kutlar, S. S. Chen, T. H. J. Huisman, P. Demuro, M. Formato, L. Manca & B. Masala. (1986) DNA polymorphisms in north Sardinian newborns and their linkage with abnormal ? globin gene arrangements and with ?o-thalassemia. Biochemical Genetics 24:9-10, pages 669-681.
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