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C Dodé

Showing results (1-10 of 35) with videos related to

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Annales D'Endocrinologie|April 6, 2010
Clinical genetics of Kallmann syndromeC Dodé, J-P Hardelin
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|November 7, 2008
The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et alJ-P Hardelin, C Dodé
British Journal of Haematology|October 1, 1990
Locus assignment of human alpha globin mutations by selective amplification and direct sequencingC Dodé, J Rochette, R Krishnamoorthy
Annales De Genetique|January 1, 1988
Types of alpha+ thalassemia in Southeast Asia refugeesC Dodé, D Labie, J Rochette
American Journal of Hematology|July 1, 1990
Level and composition of fetal hemoglobin expression in normal newborn babies are not dependent on beta cluster DNA haplotypeJ Rochette, C Dodé, F Leturcq, et al.
British Journal of Haematology|January 1, 1993
Rapid analysis of -alpha 3.7 thalassaemia and alpha alpha alpha anti 3.7 triplication by enzymatic amplification analysisC Dodé, R Krishnamoorthy, J Lamb, et al.
Human Genetics|February 1, 1988
Analysis of crossover type in the alpha -3.7 haplotype among sickle cell anemia patients from various parts of AfricaC Dodé, A Berth, J Rochette, et al.
Annales De Genetique|January 1, 1996
Sequence analysis of the CAG triplet repeats region in the Huntington disease gene (IT15) in several mammalian speciesC Pêcheux, A L Gall, J C Kaplan, et al.
La Revue De Medecine Interne|December 6, 2003
[Tumor necrosis factor receptor superfamily 1A-associated periodic syndrome (TRAPS)]V Hentgen, B Granel, C Dodé, et al.
Electrophoresis|December 1, 1989
Effect of ligand-affinity differences of human hemoglobin variants on electrophoretic behavior and their isolation and functional characterizationJ Rochette, N Deburgrave, B Bohn, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
Annales D'Endocrinologie|April 6, 2010
Clinical genetics of Kallmann syndromeC Dodé, J-P Hardelin
Sexual Development : Genetics, Molecular Biology, Evolution, Endocrinology, Embryology, and Pathology of Sex Determination and Differentiation|November 7, 2008
The complex genetics of Kallmann syndrome: KAL1, FGFR1, FGF8, PROKR2, PROK2, et alJ-P Hardelin, C Dodé
British Journal of Haematology|October 1, 1990
Locus assignment of human alpha globin mutations by selective amplification and direct sequencingC Dodé, J Rochette, R Krishnamoorthy
Annales De Genetique|January 1, 1988
Types of alpha+ thalassemia in Southeast Asia refugeesC Dodé, D Labie, J Rochette
American Journal of Hematology|July 1, 1990
Level and composition of fetal hemoglobin expression in normal newborn babies are not dependent on beta cluster DNA haplotypeJ Rochette, C Dodé, F Leturcq, et al.
British Journal of Haematology|January 1, 1993
Rapid analysis of -alpha 3.7 thalassaemia and alpha alpha alpha anti 3.7 triplication by enzymatic amplification analysisC Dodé, R Krishnamoorthy, J Lamb, et al.
Human Genetics|February 1, 1988
Analysis of crossover type in the alpha -3.7 haplotype among sickle cell anemia patients from various parts of AfricaC Dodé, A Berth, J Rochette, et al.
Annales De Genetique|January 1, 1996
Sequence analysis of the CAG triplet repeats region in the Huntington disease gene (IT15) in several mammalian speciesC Pêcheux, A L Gall, J C Kaplan, et al.
La Revue De Medecine Interne|December 6, 2003
[Tumor necrosis factor receptor superfamily 1A-associated periodic syndrome (TRAPS)]V Hentgen, B Granel, C Dodé, et al.
Electrophoresis|December 1, 1989
Effect of ligand-affinity differences of human hemoglobin variants on electrophoretic behavior and their isolation and functional characterizationJ Rochette, N Deburgrave, B Bohn, et al.
Pageof 4