Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

T Henni

Showing results (1-10 of 32) with videos related to

Pageof 4
Sort By:
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 populationT 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 populationG Kohen, N Salome, T Henni, et al.
Current Problems in Dermatology|January 1, 1990
Cutaneous pseudolymphomas: immunophenotypical and immunogenotypical studiesJ Wechsler, M Bagot, 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.
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.
British Journal of Haematology|March 1, 1985
Red cell kinetics in thalassaemia intermedia: its use for a prospective prognosisY 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 systemP Colonna, K Belhadj-Merzoug, T Henni, et al.
Human Genetics|March 1, 1987
Alpha-thalassemia haplotypes in the Algerian populationT Henni, F Morlé, B Lopez, et al.
Pageof 4

Showing results (1-10 of 32) with videos related to

Sort By:
Pageof 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 populationT 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 populationG Kohen, N Salome, T Henni, et al.
Current Problems in Dermatology|January 1, 1990
Cutaneous pseudolymphomas: immunophenotypical and immunogenotypical studiesJ Wechsler, M Bagot, 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.
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.
British Journal of Haematology|March 1, 1985
Red cell kinetics in thalassaemia intermedia: its use for a prospective prognosisY 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 systemP Colonna, K Belhadj-Merzoug, T Henni, et al.
Human Genetics|March 1, 1987
Alpha-thalassemia haplotypes in the Algerian populationT Henni, F Morlé, B Lopez, et al.
Pageof 4