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Y Le Gall

Showing results (61-70 of 84) with videos related to

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Annales De Pediatrie|December 1, 1988
[Prenatal diagnosis of mucoviscidosis using biochemical analysis of the amniotic fluid. Evaluation at the University Hospital Center of Rennes]V David, S Odent, J Van der Straeten, et al.
La Revue De Medecine Interne|June 1, 1982
[Genetic factors Bf and glyoxalase in Basedow's disease]H Allannic, R Fauchet, Y Lorcy, et al.
Human Molecular Genetics|January 1, 1993
Localization of seven new genes around the HLA-A locusA el Kahloun, B Chauvel, V Mauvieux, et al.
Human Genetics|August 1, 1990
HLA class I gene polymorphism in genetic hemochromatosisA M Jouanolle, J Yaouanq, M Blayau, et al.
Immunogenetics|January 1, 1992
A continuous restriction map from HLA-E to HLA-F. Structural comparison between different HLA-A haplotypesA el Kahloun, C Vernet, A M Jouanolle, et al.
Molecular Human Reproduction|December 2, 2000
Molecular screening of the CFTR gene in men with anomalies of the vas deferens: identification of three novel mutationsP Jézéquel, C Dubourg, D Le Lannou, et al.
Advances in Experimental Medicine and Biology|January 1, 1994
Localization of seven new genes around the HLA-A locusA el Kahloun, B Chauvel, V Mauvieux, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1984
[Abnormalities of the central nervous system. Results of 3 years of genetic counseling at the University Hospital of Rennes: 192 cases]B Le Marec, J Milon, M Catheline, et al.
Clinical Chemistry|June 1, 1995
Structural analysis of CFTR gene in congenital bilateral absence of vas deferensP Jézéquel, I Dorval, P Fergelot, et al.
Blood Cells, Molecules & Diseases|August 14, 2001
Low penetrant hemochromatosis phenotype in eight families: no evidence of modifiers in the MHC regionS Sachot, R Moirand, A M Jouanolle, et al.
Pageof 9

Showing results (61-70 of 84) with videos related to

Sort By:
Pageof 9
Annales De Pediatrie|December 1, 1988
[Prenatal diagnosis of mucoviscidosis using biochemical analysis of the amniotic fluid. Evaluation at the University Hospital Center of Rennes]V David, S Odent, J Van der Straeten, et al.
La Revue De Medecine Interne|June 1, 1982
[Genetic factors Bf and glyoxalase in Basedow's disease]H Allannic, R Fauchet, Y Lorcy, et al.
Human Molecular Genetics|January 1, 1993
Localization of seven new genes around the HLA-A locusA el Kahloun, B Chauvel, V Mauvieux, et al.
Human Genetics|August 1, 1990
HLA class I gene polymorphism in genetic hemochromatosisA M Jouanolle, J Yaouanq, M Blayau, et al.
Immunogenetics|January 1, 1992
A continuous restriction map from HLA-E to HLA-F. Structural comparison between different HLA-A haplotypesA el Kahloun, C Vernet, A M Jouanolle, et al.
Molecular Human Reproduction|December 2, 2000
Molecular screening of the CFTR gene in men with anomalies of the vas deferens: identification of three novel mutationsP Jézéquel, C Dubourg, D Le Lannou, et al.
Advances in Experimental Medicine and Biology|January 1, 1994
Localization of seven new genes around the HLA-A locusA el Kahloun, B Chauvel, V Mauvieux, et al.
Journal De Gynecologie, Obstetrique Et Biologie De La Reproduction|January 1, 1984
[Abnormalities of the central nervous system. Results of 3 years of genetic counseling at the University Hospital of Rennes: 192 cases]B Le Marec, J Milon, M Catheline, et al.
Clinical Chemistry|June 1, 1995
Structural analysis of CFTR gene in congenital bilateral absence of vas deferensP Jézéquel, I Dorval, P Fergelot, et al.
Blood Cells, Molecules & Diseases|August 14, 2001
Low penetrant hemochromatosis phenotype in eight families: no evidence of modifiers in the MHC regionS Sachot, R Moirand, A M Jouanolle, et al.
Pageof 9