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C Verlingue

Showing results (11-20 of 33) with videos related to

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Human Genetics|April 1, 1994
Retrospective study of the cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Guthrie cards from a large cohort of neonatal screening for cystic fibrosisC Verlingue, B Mercier, I Lecoq, et al.
Molecular and Cellular Probes|April 1, 1995
Identification of six novel CFTR mutations in a sample of Italian cystic fibrosis patientsC Férec, G Novelli, C Verlingue, et al.
Human Genetics|August 1, 1996
Linkage disequilibrium between the four most common cystic fibrosis mutations and microsatellite haplotypes in the Celtic population of BrittanyM De Braekeleer, A Chaventré, G Bertorelle, et al.
Nature Genetics|June 1, 1992
Detection of over 98% cystic fibrosis mutations in a Celtic populationC Férec, M P Audrezet, B Mercier, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Distribution of CFTR mutations in cystic fibrosis patients of Tunisian origin: identification of two novel mutationsT Messaoud, C Verlingue, E Denamur, et al.
Human Mutation|January 1, 1994
Identification of two novel mutations in the CFTR gene: 3007 del G and 3271 + 1 G-->AB Mercier, M P Audrézet, J Feigelson, et al.
Revue Des Maladies Respiratoires|January 1, 1989
[Mucoviscidosis: current diagnostic possibilities. Applications in perinatology]C Ferec, J J Chabaud, P Parent, et al.
Human Mutation|January 1, 1995
Complete screening of mutations in the coding sequence of the CFTR gene in a sample of CF patients from Russia: identification of three novel allelesC Verlingue, N I Kapranov, B Mercier, et al.
Clinical Genetics|April 29, 1998
Complete identification of cystic fibrosis transmembrane conductance regulator mutations in the CF population of Saguenay Lac-Saint-Jean (Quebec, Canada)M De Braekeleer, C Mari, C Verlingue, et al.
American Journal of Human Genetics|January 1, 1995
Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patientsB Mercier, C Verlingue, W Lissens, et al.
Pageof 4

Showing results (11-20 of 33) with videos related to

Sort By:
Pageof 4
Human Genetics|April 1, 1994
Retrospective study of the cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Guthrie cards from a large cohort of neonatal screening for cystic fibrosisC Verlingue, B Mercier, I Lecoq, et al.
Molecular and Cellular Probes|April 1, 1995
Identification of six novel CFTR mutations in a sample of Italian cystic fibrosis patientsC Férec, G Novelli, C Verlingue, et al.
Human Genetics|August 1, 1996
Linkage disequilibrium between the four most common cystic fibrosis mutations and microsatellite haplotypes in the Celtic population of BrittanyM De Braekeleer, A Chaventré, G Bertorelle, et al.
Nature Genetics|June 1, 1992
Detection of over 98% cystic fibrosis mutations in a Celtic populationC Férec, M P Audrezet, B Mercier, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Distribution of CFTR mutations in cystic fibrosis patients of Tunisian origin: identification of two novel mutationsT Messaoud, C Verlingue, E Denamur, et al.
Human Mutation|January 1, 1994
Identification of two novel mutations in the CFTR gene: 3007 del G and 3271 + 1 G-->AB Mercier, M P Audrézet, J Feigelson, et al.
Revue Des Maladies Respiratoires|January 1, 1989
[Mucoviscidosis: current diagnostic possibilities. Applications in perinatology]C Ferec, J J Chabaud, P Parent, et al.
Human Mutation|January 1, 1995
Complete screening of mutations in the coding sequence of the CFTR gene in a sample of CF patients from Russia: identification of three novel allelesC Verlingue, N I Kapranov, B Mercier, et al.
Clinical Genetics|April 29, 1998
Complete identification of cystic fibrosis transmembrane conductance regulator mutations in the CF population of Saguenay Lac-Saint-Jean (Quebec, Canada)M De Braekeleer, C Mari, C Verlingue, et al.
American Journal of Human Genetics|January 1, 1995
Is congenital bilateral absence of vas deferens a primary form of cystic fibrosis? Analyses of the CFTR gene in 67 patientsB Mercier, C Verlingue, W Lissens, et al.
Pageof 4