Citations (14)
Keep up to date with the latest research on this topic with citation updates for this article.
Read on this site (6)
Slaheddine Fattoum, Taeib Messaoud & Amina Bibi. (2004) Molecular Basis of β‐Thalassemia in the Population of Tunisia. Hemoglobin 28:3, pages 177-187.
Read now
Read now
Imen Chouk, Béchir Ben Daoud, Fethi Mellouli, Mohamed Bejaoui, Nathalie Gérard, Koussay Dellagi & Salem Abbes. (2004) Contribution to the Description of the β‐Thalassemia Spectrum in Tunisia and the Origin of Mutation Diversity. Hemoglobin 28:3, pages 189-195.
Read now
Read now
Amine Zorai, Cornelis L. Harteveld, Achech Bakir, Peter Van Delft, Abdelaziz Falfoul, Koussay Dellagi, Salem Abbes & Piero C. Giordano. (2002) MOLECULAR SPECTRUM OF α-THALASSEMIA IN TUNISIA: EPIDEMIOLOGY AND DETECTION AT BIRTH. Hemoglobin 26:4, pages 353-362.
Read now
Read now
G. Lacerra, G. Fioretti, A. Hani, D. Duka, M. De Angioletti, L. Pagano, A. Viola, S. Desicato, P. Ferranti, P. Pucci, E. Boletini & C. Carestia. (1993) HB O-Arab [β121(GH4)GLU→LYS]: Association with DNA Polymorphisms of African Ancestry in two Mediterranean Families. Hemoglobin 17:6, pages 523-535.
Read now
Read now
S. Fattoum, F. Guemira, C. Öner, R. Öner, H-W. Li, F. Kutlar & T. H.J. Huisman. (1991) β-Thalassemia, HB S-β-Thalassemia and Sickle Cell Anemia Among Tunisians. Hemoglobin 15:1-2, pages 11-21.
Read now
Read now
S. Abbes, S. Fattoun, N. Vidaud, M. Goossens & J. Rosa. (1991) Sickle Cell Anemia in the Tunisian Population: Haplotyping and HB F Expression. Hemoglobin 15:1-2, pages 1-9.
Read now
Read now
Articles from other publishers (8)
Emna Bouatrous, Sonia Nouira, Monia Ben Khaled, Monia Ouederni, Salem Abbes, Samia Menif & Houyem Ouragini. (2021) First Observation of HbM-Saskatoon at the Origin of Neonatal Cyanosis in a Tunisian Baby. Journal of Pediatric Hematology/Oncology 43:8, pages e1055-e1058.
Crossref
Crossref
Chaima Kasmi, Yessine Amri, Sondess Hadj-Fredj, Sabrine Oueslati, Malek Dabboussi, Rahma Mahjoub, Sana Hammami, Imen Aljane, Faika Ben Mami, Henda Jamoussi, Taieb Messaoud & Amina Bibi. (2021) Analysis of δ-globin gene alleles in Tunisians: description of three new delta-thalassemia mutations. Molecular Biology Reports 48:8, pages 5923-5933.
Crossref
Crossref
Ghazi O. Tadmouri, Konduru S. Sastry & Lotfi Chouchane. (2014) Arab gene geography: From population diversities to personalized medical genomics. Global Cardiology Science and Practice 2014:4, pages 54.
Crossref
Crossref
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.
Crossref
Crossref
Moumni Imen, Ben Mansour Mosbehi Ikbel, Chaouch Leila, Mellouli Fethi, Zorai Amine, Bejaoui Mohamed & Abbes Salem. (2011) Restriction mapping of βS locus among tunisian sickle-cell patients. American Journal of Human Biology 23:6, pages 815-819.
Crossref
Crossref
Imed Touhami, Slaheddine Fattoum, Amina Bibi, Hajer Siala, Taieb Messaoud, Donia Koubaa, Rafik Mankai, Zakia Bartagi & Daniel Le Gallais. (2009) The epidemiology of abnormal hemoglobins in Mediterranean high-level athletes. European Journal of Applied Physiology 108:6, pages 1075-1081.
Crossref
Crossref
Amel Haj Khelil, Sandrine Laradi, Abdelhedi Miled, Ghazi Omar Tadmouri, Jemni Ben Chibani & Pascale Perrin. (2004) Clinical and molecular aspects of haemoglobinopathies in Tunisia. Clinica Chimica Acta 340:1-2, pages 127-137.
Crossref
Crossref
Faouzi Baklouti, Alain Francina, Evelyne Dorléac, Véronique Baudin‐Chich, Germaine Gombaud‐Saintonge, Henri Plauchu, Henri Wajcman, Jean Delaunay & Jacqueline Godet. (2006) Asymptomatic association of hemoglobin Dunn (α6[A4]Asp→Asn) and hemoglobin O‐Arab (β121[GH4]Glu→Lys) in a Moroccan man. American Journal of Hematology 27:4, pages 253-256.
Crossref
Crossref