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hemoglobin S-beta thalassemia 相关文献:
Exagamglogene Autotemcel: First Approval.
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Sickle Cell Disease.
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2003 Sep 15 [updated 2025 Feb 13]. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Amemiya A, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2025.
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Hb S/beta-Thalassemia in the REDS-III Brazil Sickle Cell Disease Cohort: Clinical, Laboratory and Molecular Characteristics.
Belisário AR, Carneiro-Proietti AB, Sabino EC, Araújo A, Loureiro P, Máximo C, Flor-Park MV, Rodrigues DDOW, Ozahata MC, McClure C, Mota RA, Gomes Moura IC, Custer B, Kelly S; Recipient Epidemiology and Donor Evaluation Study (REDS-III) International Component Brazil.
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Compound Heterozygosity of beta-Thalassemia and the Sickle Cell Hemoglobin in Various Populations of Chhattisgarh State, India.
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The Spectrum of beta-Thalassemia Mutations in a Population from the Brazilian Amazon.
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Stratification of beta(S)beta(+) Compound Heterozygotes Based on L-Glutamine Administration and RDW: Focusing on Disease Severity.
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