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Ibrahim M Gosadi, Gassem A Gohal, Alanoud E Dalak, Anas A Alnami, Norah A Aljabri & Atyaf J Zurayyir. (2021) Assessment of Factors Associated with the Effectiveness of Premarital Screening for Hemoglobinopathies in the South of Saudi Arabia. International Journal of General Medicine 14, pages 3079-3086.
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Stamatia Theodoridou, Nikolaos Prapas, Angeliki Balassopoulou, Effrossyni Boutou, Timoleon-Achilleas Vyzantiadis, Despoina Adamidou, Evangelia-Eleni Delaki, Eleni Yfanti, Marina Economou, Αikaterini Teli, Olga Karakasidou, Evangelia Skatharoudi, Theodoros Theodoridis & Ersi Voskaridou. (2018) Efficacy of the National Thalassaemia and Sickle Cell Disease Prevention Programme in Northern Greece: 15-Year Experience, Practice and Policy Gaps for Natives and Migrants. Hemoglobin 42:4, pages 257-263.
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Sireen M. Alkhaldi, Moawia M. Khatatbeh, Vanja E.M. Berggren & Hana A. Taha. (2016) Knowledge and Attitudes Toward Mandatory Premarital Screening Among University Students in North Jordan. Hemoglobin 40:2, pages 118-124.
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Khawla M. Belhoul, Mahera Abdulrahman & Rafeeiah F. Alraei. (2013) Hemoglobinopathy Carrier Prevalence in The United Arab Emirates: First Analysis of The Dubai Health Authority Premarital Screening Program Results. Hemoglobin 37:4, pages 359-368.
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Amal El-Beshlawy & Ilham Youssry. (2009) Prevention of Hemoglobinopathies in Egypt. Hemoglobin 33:sup1, pages S14-S20.
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Articles from other publishers (6)
Md Tarikul Islam, Suprovath Kumar Sarkar, Nusrat Sultana, Mst. Noorjahan Begum, Golam Sarower Bhuyan, Shezote Talukder, A. K. M. Muraduzzaman, Md Alauddin, Mohammad Sazzadul Islam, Pritha Promita Biswas, Aparna Biswas, Syeda Kashfi Qadri, Tahmina Shirin, Bilquis Banu, Salma Sadya, Manzoor Hussain, Golam Sarwardi, Waqar Ahmed Khan, Mohammad Abdul Mannan, Hossain Uddin Shekhar, Emran Kabir Chowdhury, Abu Ashfaqur Sajib, Sharif Akhteruzzaman, Syed Saleheen Qadri, Firdausi Qadri & Kaiissar Mannoor. (2018) High resolution melting curve analysis targeting the HBB gene mutational hot-spot offers a reliable screening approach for all common as well as most of the rare beta-globin gene mutations in Bangladesh. BMC Genetics 19:1.
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Andrew Turner, Jurgen Sasse & Aniko Varadi. (2016) Rapid detection of pathological mutations and deletions of the haemoglobin beta gene (HBB) by High Resolution Melting (HRM) analysis and Gene Ratio Analysis Copy Enumeration PCR (GRACE-PCR). BMC Medical Genetics 17:1.
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F. Ouali, H. Siala, A. Bibi, S. Hadj Fredj, B. Dakhlaoui, R. Othmani, F. Ouenniche, F. Zouari, B. Bouguerra, H. Rezigua, S. Fattoum & T. Messaoud. (2016) Prenatal diagnosis of hemoglobinopathies in Tunisia: an 18 years of experience. International Journal of Laboratory Hematology 38:3, pages 223-232.
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Yupin Jopang, Suthep Petchmark, Arunee Jetsrisuparb, Kanokwan Sanchaisuriya, Pattara Sanchaisuriya & Frank Peter Schelp. (2012) Community Participation for Thalassemia Prevention Initiated by Village Health Volunteers in Northeastern Thailand. Asia Pacific Journal of Public Health 27:2, pages NP2144-NP2156.
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Fahad M. Alswaidi, Ziad A. Memish, Sarah J. O'Brien, Nasser A. Al‐Hamdan, Faisal M. Al‐Enzy, Osamah A. Alhayani & Ali M. Al‐Wadey. (2011) At‐Risk Marriages after Compulsory Premarital Testing and Counseling for β‐Thalassemia and Sickle Cell Disease in Saudi Arabia, 2005–2006. Journal of Genetic Counseling 21:2, pages 243-255.
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Nicole E Cousens, Clara L Gaff, Sylvia A Metcalfe & Martin B Delatycki. (2010) Carrier screening for Beta-thalassaemia: a review of international practice. European Journal of Human Genetics 18:10, pages 1077-1083.
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