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C Cazeneuve

Showing results (1-10 of 41) with videos related to

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Human Mutation|January 29, 2000
Screening practices for mutations in the CFTR gene ABCC7E Girodon-Boulandet, C Cazeneuve, M Goossens
Human Mutation|January 1, 1995
Mutation heterogeneity of cystic fibrosis in France: screening by denaturing gradient gel electrophoresis using psoralen-modified oligonucleotideT Bienvenu, C Cazeneuve, J C Kaplan, et al.
Annales De Genetique|January 1, 1995
Diagnostic usefulness of the polymorphism of the GT dinucleotide and the polythymidine tract in intron 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) geneC Cazeneuve, C Beldjord, J C Kaplan, et al.
Revue Neurologique|May 7, 2011
Autosomal dominant cerebellar ataxiasC Marelli, C Cazeneuve, A Brice, et al.
Journal of Medical Genetics|February 27, 2004
Subcellular localisation of marenostrin/pyrin isoforms carrying the most common mutations involved in familial Mediterranean fever in the presence or absence of its binding partner ASCC Cazeneuve, S Papin, I Jéru, et al.
Annales De Genetique|February 16, 2000
[French Society for Human Genetics. "Genetics in Practice" Commission. Core scientific data of use in genetic counseling. Familial Mediterranean fever]C Cazeneuve, C Dode, M Delpech, et al.
Revue Neurologique|January 15, 2020
Pre-symptomatic diagnosis in ALSP Corcia, S Lumbroso, C Cazeneuve, et al.
Methodsx|July 8, 2015
Methodology to study polymers interaction by surface plasmon resonance imagingN Vollmer, F Trombini, M Hely, et al.
Human Molecular Genetics|February 1, 1994
A new missense mutation (G27E) in exon 2 of the CFTR gene in a mildly affected cystic fibrosis patientT Bienvenu, C Cazeneuve, C Beldjord, et al.
Annals of the Rheumatic Diseases|January 28, 2006
Intrafamilial segregation analysis of the p.E148Q MEFV allele in familial Mediterranean feverD O Tchernitchko, M Gérard-Blanluet, M Legendre, et al.
Pageof 5

Showing results (1-10 of 41) with videos related to

Sort By:
Pageof 5
Human Mutation|January 29, 2000
Screening practices for mutations in the CFTR gene ABCC7E Girodon-Boulandet, C Cazeneuve, M Goossens
Human Mutation|January 1, 1995
Mutation heterogeneity of cystic fibrosis in France: screening by denaturing gradient gel electrophoresis using psoralen-modified oligonucleotideT Bienvenu, C Cazeneuve, J C Kaplan, et al.
Annales De Genetique|January 1, 1995
Diagnostic usefulness of the polymorphism of the GT dinucleotide and the polythymidine tract in intron 8 of the cystic fibrosis transmembrane conductance regulator (CFTR) geneC Cazeneuve, C Beldjord, J C Kaplan, et al.
Revue Neurologique|May 7, 2011
Autosomal dominant cerebellar ataxiasC Marelli, C Cazeneuve, A Brice, et al.
Journal of Medical Genetics|February 27, 2004
Subcellular localisation of marenostrin/pyrin isoforms carrying the most common mutations involved in familial Mediterranean fever in the presence or absence of its binding partner ASCC Cazeneuve, S Papin, I Jéru, et al.
Annales De Genetique|February 16, 2000
[French Society for Human Genetics. "Genetics in Practice" Commission. Core scientific data of use in genetic counseling. Familial Mediterranean fever]C Cazeneuve, C Dode, M Delpech, et al.
Revue Neurologique|January 15, 2020
Pre-symptomatic diagnosis in ALSP Corcia, S Lumbroso, C Cazeneuve, et al.
Methodsx|July 8, 2015
Methodology to study polymers interaction by surface plasmon resonance imagingN Vollmer, F Trombini, M Hely, et al.
Human Molecular Genetics|February 1, 1994
A new missense mutation (G27E) in exon 2 of the CFTR gene in a mildly affected cystic fibrosis patientT Bienvenu, C Cazeneuve, C Beldjord, et al.
Annals of the Rheumatic Diseases|January 28, 2006
Intrafamilial segregation analysis of the p.E148Q MEFV allele in familial Mediterranean feverD O Tchernitchko, M Gérard-Blanluet, M Legendre, et al.
Pageof 5