Showing results (1-10 of 37) with videos related to
Sort By:
Pageof 4
Archives De L'Institut Pasteur De Tunis|March 1, 1984
[Identification of abnormal hemoglobins by isoelectric focusing]S Abbes, S FattoumArchives De L'Institut Pasteur De Tunis|September 1, 1985
[Manipulations in genetic engineering. Consequences and fields of application]M Sellami, N Labaied, S FattoumNouvelle Revue Francaise D'Hematologie|January 1, 1986
[Alpha-thalassemia in Tunisia: molecular bases of hemoglobinosis H]S Abbes, M Vidaud, S Fattoum, et al.Archives De L'Institut Pasteur De Tunis|June 1, 1984
[Contribution of hemoglobin synthesis in vitro to the diagnosis of thalassemia]M Sellami, S Abbes, F Guemira, et al.Annales De Pediatrie|April 1, 1992
[Association of Hbo Arab/beta-thalassemia discovered fortuitously in 2 brothers]M A Mongalgi, A Debbabi, F Guemira, et al.Annales De Pediatrie|January 1, 1993
[HbC/beta-thalassemia association. Eleven cases observed in Tunisia]S Fattoum, F Guemira, M Abdennebi, et al.Archives De L'Institut Pasteur De Tunis|December 1, 1985
[Double heterozygous Hb O Arab/beta-thalassemia in a Tunisian child]F Haji, A Chadli, S Fattoum, et al.Hemoglobin|January 1, 1991
Sickle cell anemia in the Tunisian population: haplotyping and HB F expressionS Abbes, S Fattoum, M Vidaud, et al.Sante Publique (Vandoeuvre-Les-Nancy, France)|February 10, 2000
[Contributions to the sociologic analysis of the impact of sickle cell disease on families from Northern Tunisia]R Hamza, S Fattoum, M Péchevis, et al.Annals of Hematology|May 24, 2003
HbHope/HbS and HbS/beta-thal double compound heterozygosity in a Mauritanian family: clinical and biochemical studiesV M Deyde, B B Lo, T Aw, et al.Pageof 4