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Human Mutation
|
January 29, 2000
Screening practices for mutations in the CFTR gene ABCC7
E 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 oligonucleotide
T 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) gene
C Cazeneuve, C Beldjord, J C Kaplan, et al.
Revue Neurologique
|
May 7, 2011
Autosomal dominant cerebellar ataxias
C 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 ASC
C 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 ALS
P Corcia, S Lumbroso, C Cazeneuve, et al.
Methodsx
|
July 8, 2015
Methodology to study polymers interaction by surface plasmon resonance imaging
N 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 patient
T 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 fever
D O Tchernitchko, M Gérard-Blanluet, M Legendre, et al.
Page
of 5
Search research articles
Search
Showing results (1-10 of 41) with videos related to
Sort By:
Page
of 5
Human Mutation
|
January 29, 2000
Screening practices for mutations in the CFTR gene ABCC7
E 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 oligonucleotide
T 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) gene
C Cazeneuve, C Beldjord, J C Kaplan, et al.
Revue Neurologique
|
May 7, 2011
Autosomal dominant cerebellar ataxias
C 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 ASC
C 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 ALS
P Corcia, S Lumbroso, C Cazeneuve, et al.
Methodsx
|
July 8, 2015
Methodology to study polymers interaction by surface plasmon resonance imaging
N 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 patient
T 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 fever
D O Tchernitchko, M Gérard-Blanluet, M Legendre, et al.
Page
of 5