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Hemoglobin
international journal for hemoglobin research
Volume 30, 2006 - Issue 4
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Original Article

Detection of Two Rare β-Thalassemia Alleles Found in the Tunisian Population: Codon 47 (+A) and Codons 106/107 (+G)

Amina Bibi Laboratory of Clinical Biochemistry and Molecular Biology, Hôpital d'Enfants, Place Bab Saadoun, 1007, Tunis, Tunisia
,
Taieb Messaoud Laboratory of Clinical Biochemistry and Molecular Biology, Hôpital d'Enfants, Place Bab Saadoun, 1007, Tunis, Tunisia
,
Cherif Beldjord Laboratory of Biochemistry and Molecular Genetics, Hôpital Cochin-Port Royal, Paris, France
&
Slaheddine Fattoum Laboratory of Clinical Biochemistry and Molecular Biology, Hôpital d'Enfants, Place Bab Saadoun, 1007, Tunis, TunisiaCorrespondence[email protected]
Pages 437-447 | Received 10 Nov 2005, Accepted 08 May 2006, Published online: 07 Jul 2009

Citations (9)

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Nassima Boudrahem-Addour, Nadia Zidani, Nathalie Carion, Dominique Labie, Meriem Belhani & Cherif Beldjord. (2009) Molecular Heterogeneity of β-Thalassemia in Algeria: How to Face Up to a Major Health Problem. Hemoglobin 33:1, pages 24-36.
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Articles from other publishers (8)

Chaima Abdelhafidh Sahli, Ikbel Ben Salem, Latifa Jouini, Naouel Laouini, Rym Dabboubi, Sondes Hadj Fredj, Hajer Siala, Rym Othmeni, Boutheina Dakhlaoui, Slaheddine Fattoum, Amina Bibi & Taieb Messaoud. (2016) Setup of a Protocol of Molecular Diagnosis of β-Thalassemia Mutations in Tunisia using Denaturing High-Performance Liquid Chromatography (DHPLC). Journal of Clinical Laboratory Analysis 30:5, pages 392-398.
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F. Ouali, H. Siala, A. Bibi, S. Hadj Fredj, B. Dakhlaoui, R. Othmani, F. Ouenniche, F. Zouari, B. Bouguerra, H. Rezigua, S. Fattoum & T. Messaoud. (2016) Prenatal diagnosis of hemoglobinopathies in Tunisia: an 18 years of experience. International Journal of Laboratory Hematology 38:3, pages 223-232.
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Kais Douzi, Imen Moumni, Amine Zorai, Maha Ben Mustapha, Ikbel Mosbahi Ben Mansour, Chaouachi Dorra & Abbes Salem. (2015) Two new β + -thalassemia mutation [ β -56 (G → C); HBBc. −106 G → C ] and [ β −83 (G → A); HBBc. −133 G → A ] described among the Tunisian population . American Journal of Human Biology 27:5, pages 716-719.
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Chaima Abdelhafidh Sahli, Amina Bibi, Faida Ouali, Sondess Hadj Fredj, Boutheina Dakhlaoui, Rym Othmani, Naouel Laouini, Latifa Jouini, Fekria Ouenniche, Hajer Siala, Imed Touhami, Mariem Becher, Slaheddine Fattoum, Nour El Houda Toumi & Taieb Messaoud. (2013) Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia. Clinical Chemistry and Laboratory Medicine (CCLM) 51:11, pages 2115-2124.
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L. Jouini, C. A. Sahli, N. Laaouini, F. Ouali, I. Ben Youssef, B. Dakhlaoui, R. Othmeni, F. Ouennich, S. Hadj Fredj, H. Siala, M. Becher, N. E. Toumi, S. Fattoum, R. Hafsia, A. Bibi & T. Messaoud. (2013) Association between clinical expression and molecular heterogeneity in β-thalassemia Tunisian patients. Molecular Biology Reports 40:11, pages 6205-6212.
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Chaima A. Sahli, Amina Bibi, Faida Ouali, Sondess Hadj Fredj, Boutheina Dakhlaoui, Rym Othmani, Naouel Laaouini, Latifa Jouini, Fekria Ouenniche, Hajer Siala, Imed Touhami, Mariem Becher, Slaheddine Fattoum, Nour El Houda Toumi & Taieb Messaoud. (2013) Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia. Clinical Chemistry and Laboratory Medicine (CCLM) 51:8, pages 1595-1603.
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Gennaro Musollino, Gabriella Mastrolonardo, Romeo Prezioso, Leonilde Pagano, Paola Primignani, Clementina Carestia & Giuseppina Lacerra. (2012) Molecular mechanisms of a novel β-thalassaemia mutation due to the duplication of tetranucleotide ‘AGCT’ at the junction IVS-II/exon 3. Annals of Hematology 91:11, pages 1695-1701.
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Lilia Romdhane & Sonia Abdelhak. (2010) Genetic diseases in the Tunisian population. American Journal of Medical Genetics Part A 155:1, pages 238-267.
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