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Acta Haematologica|January 1, 1981
Hemoglobin Bart's in Northern AlgeriaT Henni, D Bachir, P Tabone, et al.Acta Haematologica|January 1, 1985
Alpha globin gene triplication in severe heterozygous beta thalassemiaT Henni, M Belhani, F Morle, et al.Acta Haematologica|January 1, 1981
Hemoglobin H disease from Algeria: genetic and molecular characterizationP Tabone, T Henni, M Belhani, et al.Scandinavian Journal of Haematology|April 1, 1984
Sickle cell beta-thalassaemia compared with sickle cell anaemia in AlgeriaM Belhani, L Morle, J Godet, et al.Human Genetics|March 1, 1987
Alpha-thalassemia haplotypes in the Algerian populationT Henni, F Morlé, B Lopez, et al.Human Heredity|January 1, 1984
Indirect evaluation of a gene frequency: calculation of beta-thalassemia frequency in Algeria based on associated hemoglobin variants frequencyD Bachir, M Belhani, J Godet, et al.Annales De Biologie Clinique|January 1, 1992
Quantification of red blood cell fragmentation: usefulness of heating cells and of automatic counting devicesD Guetarni, F Zerhouni, K Beldjord, et al.Biochemical and Biophysical Research Communications|May 31, 1983
Beta thalassemic mutations recognized by DNA mapping with Hph I and Rsa I in the Algerian populationG Kohen, N Salome, T Henni, et al.The EMBO Journal|May 1, 1985
alpha-Thalassaemia associated with the deletion of two nucleotides at position -2 and -3 preceding the AUG codonF Morlé, B Lopez, T Henni, et al.European Journal of Haematology|July 1, 1991
Occurrence and characteristics of hereditary spherocytosis in AlgeriaF Zerhouni, D Guetarni, T Henni, et al.Pageof 29