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Hemoglobin
international journal for hemoglobin research
Volume 10, 1986 - Issue 6
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Original Article

Haplotypes of βS Chromosomes Among Patients with Sickle Cell Anemia from Georgia

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Pages 623-642 | Received 10 Mar 1986, Accepted 23 Sep 1986, Published online: 16 Sep 2009

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Vigneshwaran Venkatesan, Saranya Srinivasan, Prathibha Babu & Saravanabhavan Thangavel. (2021) Manipulation of Developmental Gamma-Globin Gene Expression: an Approach for Healing Hemoglobinopathies. Molecular and Cellular Biology 41:1.
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M Mawanda, J M Ssenkusu, A Odiit, S Kiguli, A Muyingo*C Ndugwa. (2011) Micro-albuminuria in Ugandan children with sickle cell anaemia: a cross-sectional study. Annals of Tropical Paediatrics 31:2, pages 115-121.
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Svetlana Pulis, Christian A. Scerri, Pierre Schembri Wismayer, Ruth Galdies, Stephanie Bezzina Wettinger & Alex E. Felice. (2007) Developmental Effect of the XmnI Site on Gγ-Globin Gene Expression Among Newborn Hb F-Malta-I [Gγ117(G19)His→Arg, CAT→CGT] Heterozygotes and Adult β+-Thalassemia Homozygotes. Hemoglobin 31:1, pages 71-82.
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Amy E. Vinson, Aisha Walker, Dedrey Elam, Michele Glendenning, Ferdane Kutlar, Betsy Clair, Jeanette Harbin & Abdullah Kutlar. (2004) A Novel Approach to Rapid Determination of βS‐Globin Haplotypes: Sequencing of the Aγ‐IVS‐II Region. Hemoglobin 28:4, pages 317-323.
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L. Kéclard, V. Ollendorf, C. Berchel, H. Loret & G. Mérault. (1996) βs Haplotypes, α-Globin Gene Status, and Hematological Data of Sickle Cell Disease Patients in Guadeloupe (F.W.I.). Hemoglobin 20:1, pages 63-74.
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M. H. Steinberg. (1996) Modulation of the Phenotypic Diversity of Sickle Cell Anemia. Hemoglobin 20:1, pages 1-19.
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S. Abbes, S. Fattoun, N. Vidaud, M. Goossens & J. Rosa. (1991) Sickle Cell Anemia in the Tunisian Population: Haplotyping and HB F Expression. Hemoglobin 15:1-2, pages 1-9.
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M. M. Keeling, S. J. Bertolone, E. Baysal, Y-C. Gu, B. Cepreganova, J. B. Wilson & T. H. J. Huisman. (1991) HB Mizuho or α2β268(E12)Leu→pro in a Caucasian Boy with high levels of HB F; Identification by Sequencing of Amplified DNA. Hemoglobin 15:6, pages 477-485.
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R. B. Gupta, R. S. Tiwary, P. L. Pande, F. Kutlar, C. Öner, R. Öner & T. H. J. Huisman. (1991) Hemoglobinopathies Among the Gond Tribal Groups of Central India; Interaction of α- and β-Thalassemia with β Chain Variants. Hemoglobin 15:5, pages 441-458.
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S. K. Ballas, C. A. Talacki, K. Adachi, E. Schwartz, S. Surrey & E. Rappaport. (1991) The XMN I Site (-158, C→T) 5′ to ttle Gγ GENE: Correlation with the Senegalese Haplotype and Gγ Globin Expression. Hemoglobin 15:5, pages 393-405.
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W. A. Schroeder, Darleen R. Powars, Lois M. Kay, Linda S. Chan, Van Huynh, Joan B. Shelton & J. Roger Shelton. (1989) β-Cluster Haplotypes, α-Gene Status, and Hematological Data from SS, SC, and S-β-Thalassemia Patients in Southern California. Hemoglobin 13:4, pages 325-353.
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