Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

C Verlingue

Showing results (21-30 of 33) with videos related to

Pageof 4
Sort By:
Annales De Genetique|January 1, 1997
Clinical features of cystic fibrosis patients with rare genotypes in Saguenay Lac-Saint-Jean (Quebec, Canada)M de Braekeleer, G Mari, C Verlingue, et al.
Prenatal Diagnosis|December 1, 1993
Asymptomatic carrier of two CFTR mutations: consequences for prenatal diagnosis?C Verlingue, A David, M P Audrezet, et al.
Human Molecular Genetics|October 1, 1993
Genotype analysis of adult cystic fibrosis patientsC Férec, C Verlingue, H Guillermit, et al.
Annales De Biologie Clinique|January 1, 1994
[Cystic fibrosis gene mutations in the West of France: clinical application]C Verlingue, G Travert, M G Le Roux, et al.
Molecular and Cellular Probes|December 1, 1993
Screening for cystic fibrosis in dried blood spots of newbornsM P Audrézet, B Costes, N Ghanem, et al.
Journal of Medical Genetics|February 1, 1994
Association of 1078 del T cystic fibrosis mutation with severe diseaseP Moullier, M Jéhanne, M P Audrézet, et al.
Tissue Antigens|November 1, 1988
HLA class II genes polymorphism in DR4 giant cell arteritis patientsJ D Bignon, C Ferec, J Barrier, et al.
The New England Journal of Medicine|June 1, 1995
Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferensM Chillón, T Casals, B Mercier, et al.
Human Genetics|November 1, 1995
Neonatal screening for cystic fibrosis: result of a pilot study using both immunoreactive trypsinogen and cystic fibrosis gene mutation analysesC Férec, C Verlingue, P Parent, et al.
Clinical Genetics|February 13, 2001
Prevalence of CFTR mutations in hypertrypsinaemia detected through neonatal screening for cystic fibrosisV Scotet, M De Braekeleer, M P Audrézet, et al.
Pageof 4

Showing results (21-30 of 33) with videos related to

Sort By:
Pageof 4
Annales De Genetique|January 1, 1997
Clinical features of cystic fibrosis patients with rare genotypes in Saguenay Lac-Saint-Jean (Quebec, Canada)M de Braekeleer, G Mari, C Verlingue, et al.
Prenatal Diagnosis|December 1, 1993
Asymptomatic carrier of two CFTR mutations: consequences for prenatal diagnosis?C Verlingue, A David, M P Audrezet, et al.
Human Molecular Genetics|October 1, 1993
Genotype analysis of adult cystic fibrosis patientsC Férec, C Verlingue, H Guillermit, et al.
Annales De Biologie Clinique|January 1, 1994
[Cystic fibrosis gene mutations in the West of France: clinical application]C Verlingue, G Travert, M G Le Roux, et al.
Molecular and Cellular Probes|December 1, 1993
Screening for cystic fibrosis in dried blood spots of newbornsM P Audrézet, B Costes, N Ghanem, et al.
Journal of Medical Genetics|February 1, 1994
Association of 1078 del T cystic fibrosis mutation with severe diseaseP Moullier, M Jéhanne, M P Audrézet, et al.
Tissue Antigens|November 1, 1988
HLA class II genes polymorphism in DR4 giant cell arteritis patientsJ D Bignon, C Ferec, J Barrier, et al.
The New England Journal of Medicine|June 1, 1995
Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferensM Chillón, T Casals, B Mercier, et al.
Human Genetics|November 1, 1995
Neonatal screening for cystic fibrosis: result of a pilot study using both immunoreactive trypsinogen and cystic fibrosis gene mutation analysesC Férec, C Verlingue, P Parent, et al.
Clinical Genetics|February 13, 2001
Prevalence of CFTR mutations in hypertrypsinaemia detected through neonatal screening for cystic fibrosisV Scotet, M De Braekeleer, M P Audrézet, et al.
Pageof 4