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Hemoglobin
international journal for hemoglobin research
Volume 13, 1989 - Issue 4
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Original Article

β-Cluster Haplotypes, α-Gene Status, and Hematological Data from SS, SC, and S-β-Thalassemia Patients in Southern California

W. A. Schroeder Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, 91125
,
Darleen R. Powars Department of Pediatrics, Division of Hematology, Los Angeles, CA, 90033
,
Lois M. Kay Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, 91125
,
Linda S. Chan Divison of Biostatistics, University of Southern California School of Medicine, Los Angeles, CA, 90033
,
Van Huynh Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, 91125
,
Joan B. Shelton Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, 91125
&
J. Roger Shelton Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA, 91125
 show all
Pages 325-353 | Received 03 Jan 1989, Accepted 28 Feb 1989, Published online: 07 Jul 2009

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Kleber Yotsumoto Fertrin & Fernando Ferreira Costa. (2010) Genomic polymorphisms in sickle cell disease: implications for clinical diversity and treatment. Expert Review of Hematology 3:4, pages 443-458.
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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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Samir K. Ballas. (2001) Effect of α-Globin Genotype on the Pathophysiology of Sickle Cell Disease. Pediatric Pathology & Molecular Medicine 20:2, pages 107-121.
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S. K. Ballas, R. N. Gay & F. F. Chehab. (1997) Is Hb A2 Elevated in Adults with Sickle-A-Thalassemi (βS/βS; -α/-α). Hemoglobin 21:5, pages 405-420.
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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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M. S. Figueirido & M. H. Steinberg. (1996) 5′ Hypersensitive Site-2 and Fetal Hemogln in Brazilians. Hemoglobin 20:4, pages 435-438.
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S. H. Embury. (1995) Advances in the Prenatal and Molecular Diagnosis of the Hemoglobinopathies and Thalassemias. Hemoglobin 19:5, pages 237-261.
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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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C. A. Talacki, E. Rappaport, E. Schwartz, S. Surrey & S. K. Ballas. (1990) β-Globin Gene Cluster Haplotypes Inhbc Heterozygotes. Hemoglobin 14:3, pages 229-240.
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Alicia K. Chang, Carly C. Ginter Summarell, Parendi T. Birdie & Vivien A. Sheehan. (2018) Genetic modifiers of severity in sickle cell disease. Clinical Hemorheology and Microcirculation 68:2-3, pages 147-164.
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Françoise Bernaudin, Cécile Arnaud, Annie Kamdem, Isabelle HauFrançoise LelongRalph EpaudCorinne Pondarré & Serge Pissard. (2018) Biological impact of α genes, β haplotypes, and G6PD activity in sickle cell anemia at baseline and with hydroxyurea. Blood Advances 2:6, pages 626-637.
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Carly C Ginter Summarell & Vivien A Sheehan. (2016) Original Research: Use of hydroxyurea and phlebotomy in pediatric patients with hemoglobin SC disease. Experimental Biology and Medicine 241:7, pages 737-744.
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S.M. Hassan, M. Al Muslahi, M. Al Riyami, E. Bakker, C.L. Harteveld & P.C. Giordano. (2014) Sickle cell anemia and α-thalassemia: A modulating factor in homozygous HbS/S patients in Oman. European Journal of Medical Genetics 57:11-12, pages 603-606.
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