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Suha M. Hassan, Cornelis L. Harteveld, Egbert Bakker & Piero C. Giordano. (2015) Broader Spectrum of β-Thalassemia Mutations in Oman: Regional Distribution and Comparison with Neighboring Countries. Hemoglobin 39:2, pages 107-110.
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Mohammed Shakil Akhtar, Fuad Qaw, J. Francis Borgio, Waleed Albuali, Ahmed Suliman, Zaki Nasserullah, Sana Al-Jarrash & Amein Al-Ali. (2013) Spectrum of α-Thalassemia Mutations in Transfusion-Dependent β-Thalassemia Patients from the Eastern Province of Saudi Arabia. Hemoglobin 37:1, pages 65-73.
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Articles from other publishers (12)
Naila A. Shaheen, Hina Rehan, Areej Moghairi, Giamal Gmati, Moussab Damlaj, Hind Salama, Mushtaq Rather, May Anne Mendoza, Abeer Alanazi, Bader Al Ahmari, Mohsen Al Zahrani, Ayman Al-Hejazi & Ahmed S. Alaskar. (2022) Hematological indices in the adult saudi population: Reference intervals by gender, age, and region. Frontiers in Medicine 9.
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Nasir Al-Allawi, Sarah Al Allawi & Sana D. Jalal. (2020) Genetic epidemiology of hemoglobinopathies among Iraqi Kurds. Journal of Community Genetics 12:1, pages 5-14.
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Hayat Alafari & Faris Q. Alenzi. (2020) Biochemical and molecular analysis of the beta-globin gene and LCR region on Saudi β-thalassemia patients. Saudi Journal of Biological Sciences 27:11, pages 3106-3112.
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Riham H.N. AlMosawi, Nihad A.M. Al-Rashedi & Najla I. Ayoub. (2020) Clinical Laboratory Manifestation and Molecular Diagnosis of β-Thalassemia Patients in Iraq. Journal of Pediatric Hematology/Oncology 42:1, pages 27-31.
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Furqan Muein Auda, Afrodet A. Saleh & Dawood Salman Ali. (2019) The frequency of 6 beta-thalassemia mutations in the Iraqi patients from Najaf province. Gene Reports 17, pages 100516.
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Talal Qadah & Mohammad Sarwar Jamal. (2019)
Computational Analysis of Protein Structure Changes as a Result of Nondeletion Insertion Mutations in Human
β
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β
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Nejat Mahdieh & Bahareh Rabbani. (2016) Beta thalassemia in 31,734 cases with HBB gene mutations: Pathogenic and structural analysis of the common mutations; Iran as the crossroads of the Middle East. Blood Reviews 30:6, pages 493-508.
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J. F. Borgio, S. AbdulAzeez, Z. A. Naserullah, S. Al‐Jarrash, R. A. Al‐Ali, M. S. Al‐Madan, F. Al‐Muhanna, A. M. Al‐Suliman, A. Al‐Nafie, M. H. Steinberg & A. K. Al‐Ali. (2016) Mutations in the β‐globin gene from a Saudi population: an update. International Journal of Laboratory Hematology 38:2.
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Awatif N. Al-Nafie, J. Francis Borgio, Sayed AbdulAzeez, Ahmed M. Al-Suliman, Fuad S. Qaw, Zaki A. Naserullah, Sana Al-Jarrash, Mohammed S. Al-Madan, Rudaynah A. Al-Ali, Mohammed A. AlKhalifah, Fahad Al-Muhanna, Martin H. Steinberg & Amein K. Al-Ali. (2015) Co-inheritance of novel ATRX gene mutation and globin (α & β) gene mutations in transfusion dependent beta-thalassemia patients. Blood Cells, Molecules, and Diseases 55:1, pages 27-29.
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J. Francis Borgio, S. AbdulAzeez, Awatif N. Al-Nafie, Zaki A. Naserullah, Sana Al-Jarrash, Mohammed S. Al-Madan, Fahad Al-Muhanna, Martin H. Steinberg & Amein K. Al-Ali. (2014) A novel HBA2 gene conversion in cis or trans: “α12 allele” in a Saudi population. Blood Cells, Molecules, and Diseases 53:4, pages 199-203.
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Mohamad H Qari, Yasser Wali, Muneer H Albagshi, Mohammad Alshahrani, Azzah Alzahrani, Ibrahim A Alhijji, Abdulkareem Almomen, Abdullah Aljefri, Hussain H Al Saeed, Shaker Abdullah, Ahmad Al Rustumani, Khoutir Mahour & Shaker A Mousa. (2013) Regional consensus opinion for the management of Beta thalassemia major in the Arabian Gulf area. Orphanet Journal of Rare Diseases 8:1.
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Hanan A. Hamamy & Nasir A. S. Al-Allawi. (2012) Epidemiological profile of common haemoglobinopathies in Arab countries. Journal of Community Genetics 4:2, pages 147-167.
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