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Hemoglobin A2′ (HbA2δ′) in the Mauritanian population: first results of a preliminary survey.
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- Annals of Hematology, 2002, v. 81, n. 7, p. 386, doi. 10.1007/s00277-002-0472-5
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- Article
Epidemiological profile of hemoglobinopathies in the Mauritanian population.
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- Annals of Hematology, 2002, v. 81, n. 6, p. 320, doi. 10.1007/s00277-002-0471-6
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- Article
Prenatal diagnosis of hemoglobinopathies in Tunisia: an 18 years of experience.
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- International Journal of Laboratory Hematology, 2016, v. 38, n. 3, p. 223, doi. 10.1111/ijlh.12457
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- Article
Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients.
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- Molecular Biology Reports, 2013, v. 40, n. 11, p. 6205, doi. 10.1007/s11033-013-2732-y
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- Article
Glucose-6-phosphate dehydrogenase deficiency in Tunisia: molecular data and phenotype-genotype association.
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- Molecular Biology Reports, 2013, v. 40, n. 2, p. 851, doi. 10.1007/s11033-012-2124-8
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- Article
A point mutation in the protein 4.2 gene (allele 4.2 Tozeur) associated with hereditary haemolytic anaemia.
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- British Journal of Haematology, 1995, v. 89, n. 4, p. 762, doi. 10.1111/j.1365-2141.1995.tb08413.x
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- Article
A haemolytic syndrome associated with the complete absence of red cell membrane protein 4.2 in two Tunisian siblings.
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- British Journal of Haematology, 1990, v. 75, n. 3, p. 414, doi. 10.1111/j.1365-2141.1990.tb04357.x
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- Article
HbHope/HbS and HbS/β-thal double compound heterozygosity in a Mauritanian family: clinical and biochemical studies.
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- Annals of Hematology, 2003, v. 82, n. 7, p. 423, doi. 10.1007/s00277-003-0661-x
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- Article
α-Thalassaemia in Tunisia: some epidemiological and molecular data.
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- Journal of Genetics, 2008, v. 87, n. 3, p. 229, doi. 10.1007/s12041-008-0036-0
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- Article