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C Verlingue

Showing results (1-10 of 33) with videos related to

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Journal De Genetique Humaine|December 1, 1989
[Linkage disequilibrium and DNA markers associated with the gene for cystic fibrosis]C Ferec, C Verlingue, P Parent
Transfusion|January 1, 1988
HBV DNA in blood donorsC Ferec, C Verlingue, J P Saleum
Human Mutation|January 1, 1997
Identification of four novel mutations in the cystic fibrosis transmembrane conductance regulator gene: E664X, 2113delA, 306delTAGA, and delta M1140C Clavel, F Pennaforte, F Pigeon, et al.
Presse Medicale (Paris, France : 1983)|April 7, 1984
[Gougerot-Sjögren's syndrome. Clinical and biological correlations with the serology of Yersinia infections]J Barrier, S Robard, C Verlingue, et al.
La Nouvelle Presse Medicale|April 3, 1982
[Streptobacillus moniliformis septicemia]J J Renaut, C Pecquet, C Verlingue, et al.
Human Genetics|June 1, 1994
Identification of three novel mutations (457 TAT-->G, D192G, Q685X) in the Slovenian CF patientsM P Audrézet, N Canki-Klain, B Mercier, et al.
Archives Francaises De Pediatrie|August 1, 1990
[Direct diagnosis of predominant mutation delta F508 associated with the mucoviscidosis gene]C Férec, H Guillermit, C Verlingue, et al.
Human Molecular Genetics|January 1, 1993
Identification of 12 novel mutations in the CFTR geneM P Audrézet, B Mercier, H Guillermit, et al.
Journal of Medical Genetics|March 21, 1998
Absence of mutations in the interspecies conserved regions of the CFTR promoter region in cystic fibrosis (CF) and CF related patientsC Verlingue, S Vuillaumier, B Mercier, et al.
Fetal Diagnosis and Therapy|September 1, 1993
Prenatal diagnosis of cystic fibrosis in different European populations: application of denaturing gradient gel electrophoresisC Férec, C Verlingue, M P Audrézet, et al.
Pageof 4

Showing results (1-10 of 33) with videos related to

Sort By:
Pageof 4
Journal De Genetique Humaine|December 1, 1989
[Linkage disequilibrium and DNA markers associated with the gene for cystic fibrosis]C Ferec, C Verlingue, P Parent
Transfusion|January 1, 1988
HBV DNA in blood donorsC Ferec, C Verlingue, J P Saleum
Human Mutation|January 1, 1997
Identification of four novel mutations in the cystic fibrosis transmembrane conductance regulator gene: E664X, 2113delA, 306delTAGA, and delta M1140C Clavel, F Pennaforte, F Pigeon, et al.
Presse Medicale (Paris, France : 1983)|April 7, 1984
[Gougerot-Sjögren's syndrome. Clinical and biological correlations with the serology of Yersinia infections]J Barrier, S Robard, C Verlingue, et al.
La Nouvelle Presse Medicale|April 3, 1982
[Streptobacillus moniliformis septicemia]J J Renaut, C Pecquet, C Verlingue, et al.
Human Genetics|June 1, 1994
Identification of three novel mutations (457 TAT-->G, D192G, Q685X) in the Slovenian CF patientsM P Audrézet, N Canki-Klain, B Mercier, et al.
Archives Francaises De Pediatrie|August 1, 1990
[Direct diagnosis of predominant mutation delta F508 associated with the mucoviscidosis gene]C Férec, H Guillermit, C Verlingue, et al.
Human Molecular Genetics|January 1, 1993
Identification of 12 novel mutations in the CFTR geneM P Audrézet, B Mercier, H Guillermit, et al.
Journal of Medical Genetics|March 21, 1998
Absence of mutations in the interspecies conserved regions of the CFTR promoter region in cystic fibrosis (CF) and CF related patientsC Verlingue, S Vuillaumier, B Mercier, et al.
Fetal Diagnosis and Therapy|September 1, 1993
Prenatal diagnosis of cystic fibrosis in different European populations: application of denaturing gradient gel electrophoresisC Férec, C Verlingue, M P Audrézet, et al.
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