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Citations (21)
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Read on this site (11)
Shaima Al-Zebari, Nasir AS Al-Allawi & Farida Nerweyi. (2023) Beta Globin Gene Cluster Haplotypes in Beta Thalassemia in the Kurdistan Region of Iraq. Hemoglobin 47:3, pages 111-117.
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Chantal Farra, Lina Abdouni, Mirna Souaid, Johnny Awwad, Nadine Yazbeck & Miguel Abboud. (2021) The Spectrum of β-Thalassemia Mutations in the Population Migration in Lebanon: A 6-Year Retrospective Study. Hemoglobin 45:6, pages 365-370.
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Sulav D. Atroshi, Nasir A.S. Al-Allawi & Adil A. Eissa. (2021) Updated Molecular Spectrum of β-Thalassemia Mutations in Duhok Province, Northern Iraq: Ethnic Variation and the Impact of Immigration. Hemoglobin 45:4, pages 239-244.
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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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Figen Guzelgul, G. Seyda Seydel & Kiymet Aksoy. (2020) β-Globin Gene Mutations in Pediatric Patients with β-Thalassemia in the Region of Çukurova, Turkey. Hemoglobin 44:4, pages 249-253.
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Ahmad Shoujaa, Faten Moasses, Yasser Mukhalalaty, Hossam Murad & Faizeh Al-Quobaili. (2020) Genotype/Phenotype Correlation of β-Thalassemia in Syrian Patients: A Cross-Sectional Study. Hemoglobin 44:1, pages 42-46.
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Ahmad Shoujaa, Yasser Mukhalalaty, Hossam Murad & Faizeh Al-Quobaili. (2019) Description of a rare β-globin gene mutation, IVS-II-848 (C>A) (HBB: c.316-3C>A) in association with IVS-I-1 (G>A) (HBB: c.92 + 1G>A), observed in a Syrian family: a case report. Hemoglobin 43:4-5, pages 283-285.
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Hossam Murad & Faten Moassas. (2019) First Report on the Coinheritance of α-Thalassemia and a Rare β-Thalassemia Compound Heterozygosity for the IVS-I-I(G>A)/IVS-II-705(T>G) Mutations in a Syrian Family. Hemoglobin 43:1, pages 66-68.
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Hossam Murad, Faten Moassas, Bashar Ali & Walid Alachkar. (2019) A compound heterozygous −29 A>G and IVS-I-1 G>A mutation of HBB gene leading to β-thalassemia intermedia in a Syrian patient: A case report. Cogent Medicine 6:1.
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Hossam Murad, Faten Moassas, Ifad Ghoury & Yasser Mukhalalaty. (2018) Haplotype Analysis of Three Common β-Thalassemia Mutations in Syrian Patients. Hemoglobin 42:5-6, pages 302-305.
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Faten Moassas, Ayman Alabloog & Hossam Murad. (2018) Description of a Rare β-Globin Gene Mutation: –86 (C>G) (HBB: c.-136C>G) Observed in a Syrian Family. Hemoglobin 42:3, pages 203-205.
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Articles from other publishers (10)
Ekta Rao, Sandip Kumar Chandraker, Mable Misha Singh & Ravindra Kumar. (2024) Global distribution of β-thalassemia mutations: An update. Gene 896, pages 148022.
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Ayşe ÖZKAN, Özge ÖZALP YÜREĞİR, Banu İNCE, Bilge SARIKEPE & Özlem ANLAŞ. (2022) Tek Merkez, İki Farklı Beta Talasemili Çocuk Hasta Grubunda Beta Talasemi Mutasyonlarının ÇeşitliliğiSingle Center, Two Different Pediatric Patients with Beta Thalassemia and Diversity of Beta Thalassemia Mutations. Celal Bayar Üniversitesi Sağlık Bilimleri Enstitüsü Dergisi 9:4, pages 487-491.
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Ihab Belmokhtar, Saida Lhousni, Mounia Elidrissi Errahhali, Ayad Ghanam, Manal Elidrissi Errahhali, Zaina Sidqi, Meryem Ouarzane, Majida Charif, Mohammed Bellaoui, Redouane Boulouiz & Noufissa Benajiba. (2022) Molecular heterogeneity of β‐thalassemia variants in the Eastern region of Morocco. Molecular Genetics & Genomic Medicine 10:8.
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Zhen Wang, Wenye Sun, Huaye Chen, Yongfang Zhang, Fei Wang, Hongjian Chen, Yao Zhou, Yanhua Huang, XiXi Zhou, Qi Li & Yanlin Ma. (2021) Prevalence and molecular spectrum of α- and β-globin gene mutations in Hainan, China. International Journal of Hematology 114:3, pages 307-318.
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Ahmet Kursad Gunes & Hilmi Erdem Gozden. (2021) The Spectrum of Beta-Thalassemia Mutations in Syrian Refugees and Turkish Citizens. Cureus.
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Hossam Murad, Faten Moassas & Nour A. L. Fakseh. (2021) A rare gene variation cap +1 (A>C) (HBB: c. −50A>C) associated with codon 5 (‐CT) (HBB: c.17_18delCT) mutation in Syrian family. Molecular Genetics & Genomic Medicine 9:3.
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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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Ahmad Shoujaa, Yasser Mukhalalaty, Hossam Murad & Faizeh Al-Quobaili. (2020) A First Case of Hemoglobin Castilla [Beta 32(B14) Leu>Arg; HBB: c.98T>G] Associated with [IVS-I-1 (G>A); HBB:c.92+1G>A] Mutation Found in a Syrian Betathalassemia Patient. Thalassemia Reports 10:1, pages 8396.
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Faten Moassas, Mohamad Sayah Nweder & Hossam Murad. (2019) Hb Knossos (HBB: c.82G > T), β-globin CD 5 (−CT) (HBB: c.17_18delCT) and δ-globin CD 59 (−a) (HBD: c.179delA) mutations in a Syrian patient with β-thalassemia intermedia. BMC Pediatrics 19:1.
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Hatice Çevirici, Can Acıpayam, Ebru Dündar Yenilmez, Fatma Burcu Belen, Esra Pekpak, Yöntem Yaman & Abdullah Tuli. (2019) Investigation of beta globin gene mutations in Syrian refugee patients with thalassemia major. Turkish Journal of Biochemistry 44:2, pages 126-129.
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