Publications by authors named "Faten Moassas"

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The Spectrum of α-Thalassemia Mutations in Syrian Patients.
Hossam Murad, Faten Moassas, Bouthina Ali, Eiad Katranji, Yasser Mukhalalaty

Hemoglobin· November 2023

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Compound heterozygosity for Hb C/Hb S (HBB: c.19G>A/HBB: c.20A>T) diseases observed in a Syrian family: a case report.
Faten Moassas, Amir Daboul, Manar Assád, Hossam Murad

Ann Med Surg (Lond)· April 2023

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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.
Hossam Murad, Faten Moassas, Nour A L Fakseh

Mol Genet Genomic Med· March 2021

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Haplotype Analysis of Three Common β-Thalassemia Mutations in Syrian Patients.
Hossam Murad, Faten Moassas, Ifad Ghoury, Yasser Mukhalalaty

Hemoglobin· May 2019

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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.
Faten Moassas, Mohamad Sayah Nweder, Hossam Murad

BMC Pediatr· February 2019

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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.
Hossam Murad, Faten Moassas

Hemoglobin· January 2019

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Description of a Rare β-Globin Gene Mutation: -86 (C>G) (HBB: c.-136C>G) Observed in a Syrian Family.
Faten Moassas, Ayman Alabloog, Hossam Murad

Hemoglobin· May 2018

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Prenatal molecular diagnosis of β-thalassemia and sickle cell anemia in the Syrian population.
Hossam Murad, Faten Moassas, Rami Jarjour, Yasser Mukhalalaty, Walid Al-Achkar

Hemoglobin· July 2015

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Mutation spectrum of phenylketonuria in Syrian population: genotype-phenotype correlation.
Hossam Murad, Amir Dabboul, Faten Moassas, Diana Alasmar, Walid Al-Achkar

Gene· October 2013

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