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Poultry Science
|
May 1, 1974
Some aspects of 59Fe distribution in chicks and its incorporation into hemoglobin
J Godet, M Belhani
Soins; La Revue De Reference Infirmiere
|
July 1, 1997
[The Baye Alcoholism Center]
M Belhani, E Legallais
La Nouvelle Presse Medicale
|
June 8, 1974
[Letter: Diabetes insipidus during the development of chronic myeloid leukemia of acute outcome]
P Colonna, M Belhani
Nouvelle Revue Francaise D'Hematologie
|
July 1, 1974
[G-6PD deficiency in newborns in Algiers (author's transl)]
F Richard, M Belhani, P Colonna
Human Genetics
|
January 1, 1980
Heterogeneity in beta 0 thalassemia from Algeria: genetic, clinical and molecular studies
M Belhani, F Morlé, P Colonna, et al.
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]
|
December 1, 1977
Phenotypic variation in red cell G-6PD deficiency in heterozygotes
F Richard, M Belhani, J M Legay, 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 frequency
D Bachir, M Belhani, J Godet, et al.
Nouvelle Revue Francaise D'Hematologie
|
September 1, 1972
[Serum complement level in Hodgkin's disease]
R M Hamladji, M Belhani, J Irunberry, et al.
Acta Haematologica
|
January 1, 1981
Hemoglobin H disease from Algeria: genetic and molecular characterization
P Tabone, T Henni, M Belhani, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris
|
April 23, 1977
[1st cases of alpha-thalassemia in Algeria: 12 cases of hemoglobinosis H]
G Trabuchet, M Belhani, F Richard, et al.
Page
of 3
Search research articles
Search
Showing results (1-10 of 21) with videos related to
Sort By:
Page
of 3
Poultry Science
|
May 1, 1974
Some aspects of 59Fe distribution in chicks and its incorporation into hemoglobin
J Godet, M Belhani
Soins; La Revue De Reference Infirmiere
|
July 1, 1997
[The Baye Alcoholism Center]
M Belhani, E Legallais
La Nouvelle Presse Medicale
|
June 8, 1974
[Letter: Diabetes insipidus during the development of chronic myeloid leukemia of acute outcome]
P Colonna, M Belhani
Nouvelle Revue Francaise D'Hematologie
|
July 1, 1974
[G-6PD deficiency in newborns in Algiers (author's transl)]
F Richard, M Belhani, P Colonna
Human Genetics
|
January 1, 1980
Heterogeneity in beta 0 thalassemia from Algeria: genetic, clinical and molecular studies
M Belhani, F Morlé, P Colonna, et al.
Biomedicine / [Publiee Pour L'A.A.I.C.I.G.]
|
December 1, 1977
Phenotypic variation in red cell G-6PD deficiency in heterozygotes
F Richard, M Belhani, J M Legay, 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 frequency
D Bachir, M Belhani, J Godet, et al.
Nouvelle Revue Francaise D'Hematologie
|
September 1, 1972
[Serum complement level in Hodgkin's disease]
R M Hamladji, M Belhani, J Irunberry, et al.
Acta Haematologica
|
January 1, 1981
Hemoglobin H disease from Algeria: genetic and molecular characterization
P Tabone, T Henni, M Belhani, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris
|
April 23, 1977
[1st cases of alpha-thalassemia in Algeria: 12 cases of hemoglobinosis H]
G Trabuchet, M Belhani, F Richard, et al.
Page
of 3