Search Results - "Dakhlaoui, B."
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Prenatal diagnosis of hemoglobinopathies in Tunisia: an 18 years of experience
Published in International journal of laboratory hematology (01-06-2016)“…Summary Hemoglobinopathies are the most common genetic disease in Tunisia with a total carrier prevalence of 4.48%. Objective The aim of this study was to…”
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Journal Article -
2
Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients
Published in Molecular biology reports (01-11-2013)“…Beta-thalassemia is the most frequent hereditary blood disorder in Tunisia because of its geographic localization and history. This pathology is characterized…”
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Journal Article -
3
Prenatal diagnosis of cystic fibrosis: 10-years experience
Published in Pathologie biologie (Paris) (01-06-2015)“…We present in this study our 10years experience in prenatal diagnosis of cystic fibrosis performed in the Tunisian population. Based on family history, 40…”
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Association of TGFB1 −509C/T polymorphism gene with clinical variability in cystic fibrosis patients: A case-control study
Published in Pathologie biologie (Paris) (01-09-2015)“…In this work, we are interested to study the implication of −509C/T polymorphism, located in the promoter region of TGFB1 (transforming growth factor β1), in…”
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5
Association between clinical expression and molecular heterogeneity in [beta]-thalassemia Tunisian patients
Published in Molecular biology reports (01-11-2013)“…Beta-thalassemia is the most frequent hereditary blood disorder in Tunisia because of its geographic localization and history. This pathology is characterized…”
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Journal Article