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V Scotet

Showing results (1-10 of 17) with videos related to

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Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 17, 2020
Genetics of cystic fibrosis: BasicsC Férec, V Scotet
Molecular Genetics and Metabolism|September 26, 2000
Definition of a "functional R domain" of the cystic fibrosis transmembrane conductance regulatorJ M Chen, V Scotet, C Ferec
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 12, 2012
[Genetics and modifier genes, atypical and rare forms]C Férec, V Scotet, J Beucher, et al.
Pathologie-Biologie|January 5, 2002
[Neonatal screening for cystic fibrosis]V Scotet, M P Audrézet, M de Braekeleer, et al.
Journal of Medical Genetics|June 19, 2002
Relationship between genotype and phenotype for the CFTR gene W846X mutationI Duguépéroux, G Bellis, C Férec, et al.
British Journal of Haematology|May 19, 2004
Early onset hereditary hemochromatosis resulting from a novel TFR2 gene nonsense mutation (R105X) in two siblings of north French descentG Le Gac, F Mons, S Jacolot, et al.
Journal of Medical Genetics|September 22, 2001
Variation of iron loading expression in C282Y homozygous haemochromatosis probands and sib pairsC Mura, G Le Gac, V Scotet, et al.
Clinical Genetics|July 19, 2002
Quantification of CFTR splice variants in adults with disseminated bronchiectasis, using the TaqMan fluorogenic detection systemJ Andrieux, M P Audrézet, I Frachon, et al.
European Journal of Epidemiology|August 26, 2000
Intake of flavonoids and risk of dementiaD Commenges, V Scotet, S Renaud, et al.
Osteoarthritis and Cartilage|April 4, 2009
Do HOXB9 and COL1A1 genes play a role in congenital dislocation of the hip? Study in a Caucasian populationK Rouault, V Scotet, S Autret, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|March 17, 2020
Genetics of cystic fibrosis: BasicsC Férec, V Scotet
Molecular Genetics and Metabolism|September 26, 2000
Definition of a "functional R domain" of the cystic fibrosis transmembrane conductance regulatorJ M Chen, V Scotet, C Ferec
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|June 12, 2012
[Genetics and modifier genes, atypical and rare forms]C Férec, V Scotet, J Beucher, et al.
Pathologie-Biologie|January 5, 2002
[Neonatal screening for cystic fibrosis]V Scotet, M P Audrézet, M de Braekeleer, et al.
Journal of Medical Genetics|June 19, 2002
Relationship between genotype and phenotype for the CFTR gene W846X mutationI Duguépéroux, G Bellis, C Férec, et al.
British Journal of Haematology|May 19, 2004
Early onset hereditary hemochromatosis resulting from a novel TFR2 gene nonsense mutation (R105X) in two siblings of north French descentG Le Gac, F Mons, S Jacolot, et al.
Journal of Medical Genetics|September 22, 2001
Variation of iron loading expression in C282Y homozygous haemochromatosis probands and sib pairsC Mura, G Le Gac, V Scotet, et al.
Clinical Genetics|July 19, 2002
Quantification of CFTR splice variants in adults with disseminated bronchiectasis, using the TaqMan fluorogenic detection systemJ Andrieux, M P Audrézet, I Frachon, et al.
European Journal of Epidemiology|August 26, 2000
Intake of flavonoids and risk of dementiaD Commenges, V Scotet, S Renaud, et al.
Osteoarthritis and Cartilage|April 4, 2009
Do HOXB9 and COL1A1 genes play a role in congenital dislocation of the hip? Study in a Caucasian populationK Rouault, V Scotet, S Autret, et al.
Pageof 2