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J Godet

Showing results (11-20 of 71) with videos related to

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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.
Annales De Dermatologie Et De Venereologie|February 12, 2013
[Pseudolymphoma of the skin: ambiguous terminology: a survey among dermatologists and pathologists]E Levy, J Godet, B Cribier, 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.
Human Genetics|January 1, 1980
Heterogeneity in beta 0 thalassemia from Algeria: genetic, clinical and molecular studiesM Belhani, F Morlé, P Colonna, et al.
Annales D'Immunologie|November 1, 1976
Kinetics and biochemical properties of haemopoietic stem cells during chicken developmentJ Samarut, J P Blanchet, J Godet, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|October 1, 1994
Inducible expression of a neo gene integrated into the human alpha-globin gene clusterA Bernet-Grandaud, R Ouazana, F Morlé, et al.
The Journal of Biological Chemistry|February 12, 1998
hsp27 as a switch between differentiation and apoptosis in murine embryonic stem cellsP Mehlen, A Mehlen, J Godet, et al.
Acta Haematologica|January 1, 1984
Non-random association of the polymorphic Taq I restriction site, located 3 KB 5' to the human delta-globin gene, with the polymorphic Hind III sites within the G gamma- and A gamma-globin genesD Poncet, N Salomé, G Kohen, 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.
Human Genetics|March 1, 1987
Alpha-thalassemia haplotypes in the Algerian populationT Henni, F Morlé, B Lopez, et al.
Pageof 8

Showing results (11-20 of 71) with videos related to

Sort By:
Pageof 8
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.
Annales De Dermatologie Et De Venereologie|February 12, 2013
[Pseudolymphoma of the skin: ambiguous terminology: a survey among dermatologists and pathologists]E Levy, J Godet, B Cribier, 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.
Human Genetics|January 1, 1980
Heterogeneity in beta 0 thalassemia from Algeria: genetic, clinical and molecular studiesM Belhani, F Morlé, P Colonna, et al.
Annales D'Immunologie|November 1, 1976
Kinetics and biochemical properties of haemopoietic stem cells during chicken developmentJ Samarut, J P Blanchet, J Godet, et al.
Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|October 1, 1994
Inducible expression of a neo gene integrated into the human alpha-globin gene clusterA Bernet-Grandaud, R Ouazana, F Morlé, et al.
The Journal of Biological Chemistry|February 12, 1998
hsp27 as a switch between differentiation and apoptosis in murine embryonic stem cellsP Mehlen, A Mehlen, J Godet, et al.
Acta Haematologica|January 1, 1984
Non-random association of the polymorphic Taq I restriction site, located 3 KB 5' to the human delta-globin gene, with the polymorphic Hind III sites within the G gamma- and A gamma-globin genesD Poncet, N Salomé, G Kohen, 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.
Human Genetics|March 1, 1987
Alpha-thalassemia haplotypes in the Algerian populationT Henni, F Morlé, B Lopez, et al.
Pageof 8