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Multiplex Minisequencing of the HBB Gene: A Rapid Strategy to Confirm the Most Frequent β-Thalassemia Mutations in the Tunisian Population
by
Ben Charfeddine, Ilhem
,
Ben Lazreg, Taheni
,
M'sakni, Ahlem
,
Amara, Abdelbasset
,
Mlika, Adnène
,
Chaïeb, Anouar
,
Hlel, Khalid
,
Zouari, Noura
,
Zbidi, Faïza
,
Bouguila, Jihène
,
Soyah, Najla
,
Ayedi, Abdelkarim
,
Ben Hamouda, Hechmi
,
Abroug, Saoussen
,
Boughamoura, Lamia
,
Saad, Ali
,
Gribaa, Moez
Published in
Hemoglobin
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Journal Title
Hemoglobin
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Subjects
Beta-Globins - Genetics
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Beta-Thalassemia - Epidemiology
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Beta-Thalassemia - Genetics
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Biochemistry & Molecular Biology
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Genetic Counseling
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Genotype
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Hbb Gene
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Hematology
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Humans
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Life Sciences & Biomedicine
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Mutation
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Mutation Screening
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Phenotype
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Science & Technology
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Sequence Analysis, Dna
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Tunisia - Epidemiology
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Β-Thalassemia
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Taylor And Francis:jisc Collections:taylor And Francis Read And Publish Agreement 2024-2025:Medical Collection (Reading List)
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