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Hemoglobin
international journal for hemoglobin research
Volume 40, 2016 - Issue 1
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Short Communication

Hereditary Persistence of Fetal Hemoglobin Caused by Single Nucleotide Promoter Mutations in Sickle Cell Trait and Hb SC Disease

Anthony O. AkinbamiDepartment of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA
,
Andrew D. CampbellDepartment of Pediatrics, University of Michigan, Ann Arbor, Michigan, USA
,
Zeqiu J. HanQuest Diagnostics Nichols Institute, Chantilly, Virginia, USA
,
Hong-Yuan LuoDepartment of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA
,
David H.K. ChuiDepartment of Medicine, Boston University School of Medicine, Boston, Massachusetts, USA
&
Martin H. SteinbergDepartment of Medicine, Boston University School of Medicine, Boston, Massachusetts, USACorrespondence[email protected]
Pages 64-65 | Received 28 May 2015, Accepted 31 Jul 2015, Published online: 15 Sep 2015

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Ahmad Tamaddoni, Sahar Khabaz Astaneh, Reza Tabaripour & Haleh Akhavan-Niaki. (2019) Krüppel-Like Factor 1 Gene Mutations in Thalassemia Patients from North Iran: Report of a New Mutation Associated with β-Thalassemia Intermedia. Hemoglobin 43:1, pages 12-17.
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Articles from other publishers (3)

Caterina Minniti, Carlo Brugnara & Martin H. Steinberg. (2022) HbSC disease: A time for progress . American Journal of Hematology 97:11, pages 1390-1393.
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Martin H. Steinberg. (2020) Fetal Hemoglobin in Sickle Hemoglobinopathies: High HbF Genotypes and Phenotypes. Journal of Clinical Medicine 9:11, pages 3782.
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Carroll Flansburg, Christina M. Balentine, Ryan W. Grieger, Justin Lund, Michelle Ciambella, Deandre White, Eric Coris, Eduardo Gonzalez, Anne C. Stone & Lorena Madrigal. (2019) Fetal Hemoglobin Modulators May Be Associated With Symptomology of Football Players with Sickle Cell Trait. Southern Medical Journal 112:5, pages 289-294.
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