Compound Heterozygous Sickle Cell-Beta Thalassemia Presenting As Chronic Hemolytic Anemia With Microcytosis and Prominent Left Ventricular Trabeculation: A Case Report. [PDF]
Radhakrishnan VK +4 more
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CRISPR-Cas9-Mediated Gene Editing in Hematological Disorders: Advancing Translational and Clinical Applications. [PDF]
Singh A +5 more
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A new 308 A-G substitution in HBG2 in an acyanotic newborn: case report. [PDF]
Pellicani S +5 more
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High-performance liquid chromatography screening reveals HbS/β+-thalassemia double heterozygosity as a pediatric muscular dystrophy mimic. [PDF]
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Birth Prevalence of Sickle Cell Disease in India: A Systematic Review and Meta-Analysis. [PDF]
Rahiman EA, Anne RP, Warrier RP.
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Targeted protein degradation for fetal hemoglobin induction: a new paradigm in β-hemoglobinopathy therapy. [PDF]
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Prenatal Diagnosis of Compound Heterozygous Beta-Thalassemia: A Report of Two Cases. [PDF]
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