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Journal of Genetics|January 17, 2009
alpha-Thalassaemia in Tunisia: some epidemiological and molecular dataH Siala, F Ouali, T Messaoud, et al.Annales De Pediatrie|September 1, 1990
[Thalassemia intermedia. Report of two cases]F Khaldi, F Hassine, F Guemira, et al.Annales De Pediatrie|June 1, 1992
[HbD Iran-beta-thalassemia association in a Tunisian family]F Guemira, S Abbes, R Ducrocq, et al.Archives De L'Institut Pasteur De Tunis|January 1, 1995
[Analysis of glycosylated A1c hemoglobin by liquid phase chromatography and immunoagglutination]M Sellami, N Labaied, A Ghanem, et al.Hematology and Cell Therapy|July 1, 1996
Abnormalities of coagulation and fibrinolysis in homozygous sickle cell diseaseB Nsiri, N Gritli, F Bayoudh, et al.Hematology and Cell Therapy|December 13, 1997
Fibrinolytic response to venous occlusion in patients with homozygous sickle cell diseaseB Nsiri, N Gritli, C Mazigh, et al.Annals of Hematology|August 20, 2002
Hemoglobin A2' (HbA2delta') in the Mauritanian population: first results of a preliminary surveyV M Deyde, S Fattoum, B B Lo, et al.Archives De L'Institut Pasteur De Tunis|July 1, 1987
[A case of hemoglobin D Punjab in Tunisia. Characterization and structural study]F Guemira, F Hajji, M Sellami, et al.Annals of Hematology|July 11, 2002
Epidemiological profile of hemoglobinopathies in the Mauritanian populationV M Deyde, B B Lo, I O Khalifa, et al.Annales De Biologie Clinique|December 7, 2005
[Molecular epidemiology of cystic fibrosis in Tunisia]T Messaoud, S Bel Haj Fredj, A Bibi, et al.Pageof 4