Search Results - "Dakhlaoui, B"

Prenatal diagnosis of hemoglobinopathies in Tunisia: an 18 years of experience by Ouali, F., Siala, H., Bibi, A., Hadj Fredj, S., Dakhlaoui, B., Othmani, R., Ouenniche, F., Zouari, F., Bouguerra, B., Rezigua, H., Fattoum, S., Messaoud, T.

“…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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Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients by Jouini, L., Sahli, C. A., Laaouini, N., Ouali, F., Youssef, I. Ben, Dakhlaoui, B., Othmeni, R., Ouennich, F., Fredj, S. Hadj, Siala, H., Becher, M., Toumi, N. E., Fattoum, S., Hafsia, R., Bibi, A., Messaoud, T.

“…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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Prenatal diagnosis of cystic fibrosis: 10-years experience by Hadj Fredj, S., Ouali, F., Siala, H., Bibi, A., Othmani, R., Dakhlaoui, B., Zouari, F., Messaoud, T.

“…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 by Oueslati, S., Hadj Fredj, S., Dakhlaoui, B., Othmani, R., Siala, H., Messaoud, T.

“…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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Association between clinical expression and molecular heterogeneity in [beta]-thalassemia Tunisian patients by Jouini, L, Sahli, C A, Laaouini, N, Ouali, F, Youssef, I Ben, Dakhlaoui, B, Othmeni, R, Ouennich, F, Fredj, S Hadj, Siala, H, Becher, M, Toumi, N E, Fattoum, S, Hafsia, R, Bibi, A, Messaoud, T

“…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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