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September 25, 2026Hemoglobin

Evaluation of a Customized RDB-FTH Panel for β-Globin Variants in a Malaysian Tertiary Center

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Authors

NJNorunaluwar JalilRARaja Zahratul AzmaHAHafiza Alaudin

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Cite This Study

Jalil et al. (2026) studied this question.

synapsesocial.com/papers/6ab60ebd406bf401c14673d1https://doi.org/10.1080/03630269.2026.2732039
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Molecular spectrum and carrier frequency of deletional hereditary persistence of fetal hemoglobin and delta-beta thalassemia in Malaysia2025
  2. 2Cascade Screening of β-Thalassemia in an Indian Family Using Flow Injection Analysis–Triple Quadrupole Mass Spectrometry: Comparison of Micro Sampling Approaches with Conventional Electrophoresis2026
  3. 3Common hemoglobin variants affecting the diagnosis of β-thalassemia: A large cohort data at a single center2026 · 1 citations
  4. 4Molecular Biomarkers for Prenatal Diagnosis of Beta-Thalassemia at Hyderabad Sindh2023
  5. 5Compound heterozygosity for Southeast Asian hereditary persistence of fetal hemoglobin and β0-thalassemia results in thalassemia intermedia: Pedigree analysis and genetic research in a family from South China. A case report2024