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Results of search for 'au:"Moassas, Faten"'
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Authors
Al-Achkar, Walid
Alabloog, Ayman
Alasmar, Diana
Dabboul, Amir
Ghoury, Ifad
Jarjour, Rami
Moassas, Faten
Mukhalalaty, Yasser
Murad, Hossam
Nweder, Mohamad Sayah
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Topics
Adolescent
Adult
Child
DNA Mutational Analysis
Family
Female
Haplotypes
Heterozygote
Humans
Male
Mutation
Polymorphism, Restriction Fragment Length
Pregnancy
Prenatal Diagnosis
Syria
beta-Globins
beta-Thalassemia
blood
epidemiology
genetics
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English
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1.
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.
[electronic resource]
by
Murad, Hossam
Moassas, Faten
Producer:
20191125
In:
Hemoglobin
vol. 43
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2.
Description of a Rare β-Globin Gene Mutation: -86 (C>G) (HBB: c.-136C>G) Observed in a Syrian Family.
[electronic resource]
by
Moassas, Faten
Alabloog, Ayman
Murad, Hossam
Producer:
20190102
In:
Hemoglobin
vol. 42
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3.
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.
[electronic resource]
by
Moassas, Faten
Nweder, Mohamad Sayah
Murad, Hossam
Producer:
20200304
In:
BMC pediatrics
vol. 19
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4.
Haplotype Analysis of Three Common β-Thalassemia Mutations in Syrian Patients.
[electronic resource]
by
Murad, Hossam
Moassas, Faten
Ghoury, Ifad
Mukhalalaty, Yasser
Producer:
20190514
In:
Hemoglobin
vol. 42
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5.
Mutation spectrum of phenylketonuria in Syrian population: genotype-phenotype correlation.
[electronic resource]
by
Murad, Hossam
Dabboul, Amir
Moassas, Faten
Alasmar, Diana
Al-Achkar, Walid
Producer:
20131105
In:
Gene
vol. 528
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6.
Prenatal molecular diagnosis of β-thalassemia and sickle cell anemia in the Syrian population.
[electronic resource]
by
Murad, Hossam
Moassas, Faten
Jarjour, Rami
Mukhalalaty, Yasser
Al-Achkar, Walid
Producer:
20150708
In:
Hemoglobin
vol. 38
Online resources:
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