Citations (53)
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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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Hossam Murad, Faten Moasses, Amir Dabboul, Yasser Mukhalalaty, Ahmad Omar Bakoor, Walid Al-Achkar & Rami A. Jarjour. (2018) Geographical distribution of β-globin gene mutations in Syria. Hematology 23:9, pages 697-704.
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Martha Bravo-Urquiola, Anabel Arends, Gilberto Gómez, Silvia Montilla, Nathalie Gerard, Marycarmen Chacin, Tsouria Berbar, Odalis García, Gloria García, Dalia Velasquez, Omar Castillo & Rajagopal Krishnamoorthy. (2012) Molecular Spectrum of β-Thalassemia Mutations in the admixed Venezuelan population, and their linkage to β-Globin Gene Haplotypes. Hemoglobin 36:3, pages 209-218.
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Paloma Ropero, Silvia de la Iglesia, Jose M. Calvo-Villas, Fernando Ataúlfo González, Rosa Paúl & Ana Villegas. (2008) Origin of the Frameshift Codons 41/42 (–TCTT) Mutation in the First Cases Described in the Spanish Population. Hemoglobin 32:5, pages 513-519.
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