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Hemoglobin
international journal for hemoglobin research
Volume 34, 2010 - Issue 6
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Original Article

β-Globin Gene Haplotypes Linked with the Hb D-Punjab [β121(GH4)Glu→Gln, GAA>CAA] Mutation in Eastern India

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Pages 530-537 | Received 31 Mar 2010, Accepted 20 Apr 2010, Published online: 15 Nov 2010

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Snehadhini Dehury, Pradeep K. Mohanty, Siris Patel, Satyabrata Meher, Kishalaya Das, Prasanta Purohit, Sarmila Sahoo & Jagnyeswar Ratha. (2021) Profiling of 35 Cases of Hb S/Hb E (HBB: c.20A>T/HBB: c.79G>a), Disease and Association with α-Thalassemia and β-Globin Gene Cluster Haplotypes from Odisha, India. Hemoglobin 45:6, pages 380-386.
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Articles from other publishers (10)

Pramita Sahu, Prasanta Purohit, Santwana Mantri, Ramray Tudu, Jayanti Nayak, Sunil Kumar Agrawalla, Samira Kumar Behera, Manoj Kumar Patro, Nivedita Karmee, Diptimayee Tripathy, Bharati MishraDebi Prasad Mishra. (2021) Spectrum of hemoglobin disorders in southern Odisha, India: a hospital based study. Porto Biomedical Journal 6:1, pages e126.
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Onur Ozturk, Sanem Arikan, Ayfer Atalay & Erol O. Atalay. (2018) Time estimations by network of beta globin gene cluster haplotypes linked with Hb D-Los Angeles [β121 (GH4) Glu → Gln GAA → CAA] mutation in the world populations. Molecular Genetics & Genomic Medicine 6:6, pages 1181-1187.
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Pradeep Kumar Mohanty & Srinibas Meher. (2018) MORTALITY RISK FACTORS IN HOSPITALISED LATE ADOLESCENT AND ADULT SICKLE CELL DISEASE PATIENTS. Journal of Evidence Based Medicine and Healthcare 5:2, pages 135-139.
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Paulo do Val Rezende, Kenia da Silva Costa, Jose Carlos Domingues Junior, Paula Barezani Silveira, André Rolim Belisário, Celia Maria Silva & Marcos Borato Viana. (2016) Clinical, hematological and genetic data of a cohort of children with hemoglobin SD. Revista Brasileira de Hematologia e Hemoterapia 38:3, pages 240-246.
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Onur Ozturk, Sanem Arikan, Ayfer Atalay & Erol O. Atalay. (2016) Analysis of the population genetic structure of Hb D-Los Angeles [β121 (GH4) Glu→Gln G AA→ C AA] in Denizli, Turkey; genetic diversity, historical demography and estimation of the mutation rates based on haplotype variation . American Journal of Human Biology 28:4, pages 476-483.
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Karina Rodríguez-Capote, Mathew P. Estey, Vilte Barakauskas, Pierre Bordeleau, Cathie-Lou Christensen, Peter Zuberbuhler & Trefor N. Higgins. (2015) A novel double heterozygous Hb Fontainebleau/HbD Punjab hemoglobinopathy. Clinical Biochemistry 48:13-14, pages 904-907.
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Lidiane de Souza Torres, Jéssika Viviani Okumura, Danilo Grünig Humberto da Silva & Claudia Regina Bonini-Domingos. (2015) Hemoglobin D-Punjab: origin, distribution and laboratory diagnosis. Revista Brasileira de Hematologia e Hemoterapia 37:2, pages 120-126.
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D. K. Patel, P. Purohit, S. Dehury, P. Das, A. Dutta, S. Meher, S. Patel, S. Bag, R. S. Mashon & K. Das. (2014) Fetal hemoglobin and alpha thalassemia modulate the phenotypic expression of HbSD-Punjab. International Journal of Laboratory Hematology 36:4, pages 444-450.
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Siris Patel, Prasanta Purohit, Ranjeet Singh Mashon, Snehadhini Dehury, Satyabrata Meher, Sulia Sahoo, Subhransu Sekhar Dash, Kishalaya Das, Padmalaya Das & Dilip Kumar Patel. (2014) The effect of hydroxyurea on compound heterozygotes for sickle cell-hemoglobin D-Punjab-A single centre experience in eastern India. Pediatric Blood & Cancer 61:8, pages 1341-1346.
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Khushnooma Italia, Dipti Upadhye, Pooja Dabke, Harshada Kangane, Stacy Colaco, Pratibha Sawant, Anita Nadkarni, Ajit Gorakshakar, Dipty Jain, Yazdi Italia, Kanjaksha Ghosh & Roshan Colah. (2014) Clinical and hematological presentation among Indian patients with common hemoglobin variants. Clinica Chimica Acta 431, pages 46-51.
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