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Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]
|
July 1, 1981
Association of the sickle hemoglobin mutation with the variant 13 Kb Hpa I DNA fragment in the Algerian population
T Henni, L Morle, N Alloisio
Biochemical and Biophysical Research Communications
|
May 31, 1983
Beta thalassemic mutations recognized by DNA mapping with Hph I and Rsa I in the Algerian population
G Kohen, N Salome, T Henni, et al.
Current Problems in Dermatology
|
January 1, 1990
Cutaneous pseudolymphomas: immunophenotypical and immunogenotypical studies
J Wechsler, M Bagot, T Henni, et al.
European Journal of Haematology
|
July 1, 1991
Occurrence and characteristics of hereditary spherocytosis in Algeria
F Zerhouni, D Guetarni, 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 codon
F Morlé, B Lopez, T Henni, et al.
British Journal of Haematology
|
March 1, 1985
Red cell kinetics in thalassaemia intermedia: its use for a prospective prognosis
Y Najean, F Deschryver, T Henni, et al.
Pathologie-Biologie
|
January 1, 1988
[Detection of residual disease in onco-hematology: the contribution of molecular biology]
T Henni, M Vidaud, S Bretagne, et al.
La Nouvelle Presse Medicale
|
March 13, 1976
[Letter: Erythrocyte glucose-6-phosphate dehydrogenase (G-6PD) in thyroid disorders]
F Z Kherci, T Henni, F Richard, et al.
Acta Haematologica
|
January 1, 1988
Changes in patterns of Hodgkin's disease in Algeria, 1966-1985: influence of health care delivery system
P Colonna, K Belhadj-Merzoug, T Henni, et al.
Human Genetics
|
March 1, 1987
Alpha-thalassemia haplotypes in the Algerian population
T Henni, F Morlé, B Lopez, et al.
Page
of 4
Search research articles
Search
Showing results (1-10 of 32) with videos related to
Sort By:
Page
of 4
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]
|
July 1, 1981
Association of the sickle hemoglobin mutation with the variant 13 Kb Hpa I DNA fragment in the Algerian population
T Henni, L Morle, N Alloisio
Biochemical and Biophysical Research Communications
|
May 31, 1983
Beta thalassemic mutations recognized by DNA mapping with Hph I and Rsa I in the Algerian population
G Kohen, N Salome, T Henni, et al.
Current Problems in Dermatology
|
January 1, 1990
Cutaneous pseudolymphomas: immunophenotypical and immunogenotypical studies
J Wechsler, M Bagot, T Henni, et al.
European Journal of Haematology
|
July 1, 1991
Occurrence and characteristics of hereditary spherocytosis in Algeria
F Zerhouni, D Guetarni, 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 codon
F Morlé, B Lopez, T Henni, et al.
British Journal of Haematology
|
March 1, 1985
Red cell kinetics in thalassaemia intermedia: its use for a prospective prognosis
Y Najean, F Deschryver, T Henni, et al.
Pathologie-Biologie
|
January 1, 1988
[Detection of residual disease in onco-hematology: the contribution of molecular biology]
T Henni, M Vidaud, S Bretagne, et al.
La Nouvelle Presse Medicale
|
March 13, 1976
[Letter: Erythrocyte glucose-6-phosphate dehydrogenase (G-6PD) in thyroid disorders]
F Z Kherci, T Henni, F Richard, et al.
Acta Haematologica
|
January 1, 1988
Changes in patterns of Hodgkin's disease in Algeria, 1966-1985: influence of health care delivery system
P Colonna, K Belhadj-Merzoug, T Henni, et al.
Human Genetics
|
March 1, 1987
Alpha-thalassemia haplotypes in the Algerian population
T Henni, F Morlé, B Lopez, et al.
Page
of 4