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PRESENTED AT THE INTERNATIONAL CONFERENCE ON HEMOGLOBIN DISORDERS, KUWAIT, February 5–7th, 2011

Molecular Basis of β-Thalassemia in the United Arab Emirates

Pages 581-588 | Received 09 Sep 2011, Accepted 09 Sep 2011, Published online: 10 Nov 2011

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Aisha Moeen Khan, Asma Mohammed Al-Sulaiti, Salma Younes, Mohamed Yassin & Hatem Zayed. (2021) The spectrum of beta-thalassemia mutations in the 22 Arab countries: a systematic review. Expert Review of Hematology 14:1, pages 109-122.
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Hamda Al Dhaheri & Sehjeong Kim. (2018) The Effectiveness of Thalassemia Control Measures in the United Arab Emirates. The Effectiveness of Thalassemia Control Measures in the United Arab Emirates.
Adekunle D. Adekile, Nagihan Akbulut, Asmaa F. Azab, Sundus Al-Sharida & Diana Thomas. (2017) The Sickle β-Thalassemia Phenotype. Journal of Pediatric Hematology/Oncology 39:5, pages 327-331.
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Sehjeong Kim & Abdessamad Tridane. (2017) Thalassemia in the United Arab Emirates: Why it can be prevented but not eradicated. PLOS ONE 12:1, pages e0170485.
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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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Srdjan Denic, Mukesh M. Agarwal, Bayan Al Dabbagh, Awad El Essa, Mohamed Takala, Saad Showqi & Javed Yassin. (2013) Hemoglobin A 2 Lowered by Iron Deficiency and α -Thalassemia: Should Screening Recommendation for β -Thalassemia Change? . ISRN Hematology 2013, pages 1-5.
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