Evaluation of in silico predictors on short nucleotide variants in HBA1 , HBA2 , and HBB associated with haemoglobinopathies von Tamana, Stella, Xenophontos, Maria, Minaidou, Anna, Stephanou, Coralea, Harteveld, Cornelis L, Bento, Celeste, Traeger-Synodinos, Joanne, Fylaktou, Irene, Yasin, Norafiza Mohd, Abdul Hamid, Faidatul Syazlin, Esa, Ezalia, Halim-Fikri, Hashim, Zilfalil, Bin Alwi, Kakouri, Andrea C, Kleanthous, Marina, Kountouris, Petros

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Characterization of New Alpha Zero (α 0 ) Thalassaemia Deletion (-- GB ) among Malays in Malaysian Population von Yasin, Norafiza Mohd, Abdul Hamid, Faidatul Syazlin, Hassan, Syahzuwan, Mat Yusoff, Yuslina, Mohd Sahid, Ermi Neiza, Esa, Ezalia

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Rare coinheritance of hemoglobin vancleave with severe beta-thalassemia mutation in a patient with secondary erythrocytosis von Aziz, Nur Aisyah, Musa, Nurul Hidayah, Mathews, Melina, Rajenderan, Komalah Thevii, Abdul Hamid, Faidatul Syazlin, Hassan, Syahzuwan, Omar, Syahira Lazira, Wan Yusoff, Wan Nurul Afiqha Binti, Mohd Din, Melanie Ling Binti, Jamaludin, Nurul Amira Binti, Wan Taib, Wan Rohani, Esa, Ezalia, Mohd Yasin, Norafiza

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Rare cause of transfusion‐dependent hemolytic anemia: A case report of HbE/Hb Nottingham and literature review von Aziz, Aisyah, Baharin, Mohd Farid, Fauzi, Muhammad Yusri, Abdul Hamid, Faidatul Syazlin, Nadarajaw, Thiyagar, Ahmad, Rahimah, Hashim, Hafizah

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Next-Generation Sequencing (NGS) and Third-Generation Sequencing (TGS) for the Diagnosis of Thalassemia von Hassan, Syahzuwan, Bahar, Rosnah, Johan, Muhammad Farid, Mohamed Hashim, Ezzeddin Kamil, Abdullah, Wan Zaidah, Esa, Ezalia, Abdul Hamid, Faidatul Syazlin, Zulkafli, Zefarina

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Clinical and haematological characteristics of 38 individuals with Hb G-Makassar in Malaysia von Esa, Ezalia, Mohamad, Ahmad Sabry, Hamzah, Roszymah, Hamid, Faidatul Syazlin Abdul, Aziz, Nur Aisyah, Sevaratnam, Veena, Sathar, Jameela, Chen, Guo, Yasin, Norafiza Mohd

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A Novel Single Gene Deletion (−αMAL3.5) Giving Rise to Silent α Thalassemia Carrier Removing the Entire HBA2 Gene Observed in Two Chinese Patients with Hb H Disease: Case Report of... von Abdul Hamid, Faidatul Syazlin, Ahmad, Rahimah, Saleem, Mohamed, Aziz, Nur Aisyah, Omar, Syahira Lazira, Mohamad Arif, Siti Hida Hajira, Sathar, Jameela, Zakaria, Zubaidah

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An insight of -50 (G>A) mutation in the direct repeat element of the β-globin gene: From Malaysian perspective von Yasin, Norafiza Mohd, Hamid, Faidatul Syazlin Abdul, Hassan, Syahzuwan, Ysoff, Yuslina Mat, Sahid, Ermi Neiza Mohd, Esa, Ezalia

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Molecular and hematological studies in a cohort of beta zero South East Asia deletion (β°-thal SEA) from Malaysian perspective von Yasin, Norafiza Mohd, Abdul Hamid, Faidatul Syazlin, Hassan, Syahzuwan, Sudin, Aziee, Yassim, Haiyuni, Mohd Sahid, Ermi Neiza, Mat Yusoff, Yuslina, Esa, Ezalia, Saleem, Mohamed

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Characterization of New Alpha Zero among Malays in Malaysian Population von Yasin, Norafiza Mohd, Abdul Hamid, Faidatul Syazlin, Hassan, Syahzuwan, Mat Yusoff, Yuslina, Mohd Sahid, Ermi Neiza, Esa, Ezalia

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Next-Generation Sequencing for the Diagnosis of Thalassemia von Hassan, Syahzuwan, Bahar, Rosnah, Johan, Muhammad Farid, Mohamed Hashim, Ezzeddin Kamil, Abdullah, Wan Zaidah, Esa, Ezalia, Abdul Hamid, Faidatul Syazlin, Zulkafli, Zefarina

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