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V Scotet

Showing results (11-20 of 17) with videos related to

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Journal of Medical Genetics|June 19, 2002
Prenatal detection of cystic fibrosis by ultrasonography: a retrospective study of more than 346 000 pregnanciesV Scotet, M De Braekeleer, M P Audrézet, et al.
Osteoarthritis and Cartilage|July 17, 2010
Evidence of association between GDF5 polymorphisms and congenital dislocation of the hip in a Caucasian populationK Rouault, V Scotet, S Autret, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 25, 2020
Penetrance is a critical parameter for assessing the disease liability of CFTR variantsA Boussaroque, M-P Audrézet, C Raynal, 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.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 21, 2005
[Neonatal screening of cystic fibrosis: diagnostic and ethical problems with mild mutations]M Roussey, A Le Bihannic, M P Audrezet, et al.
Journal of Inherited Metabolic Disease|July 17, 2007
Neonatal screening of cystic fibrosis: diagnostic problems with CFTR mild mutationsM Roussey, A Le Bihannic, V Scotet, et al.
Lancet (London, England)|October 7, 2000
Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosisV Scotet, M de Braekeleer, M Roussey, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Journal of Medical Genetics|June 19, 2002
Prenatal detection of cystic fibrosis by ultrasonography: a retrospective study of more than 346 000 pregnanciesV Scotet, M De Braekeleer, M P Audrézet, et al.
Osteoarthritis and Cartilage|July 17, 2010
Evidence of association between GDF5 polymorphisms and congenital dislocation of the hip in a Caucasian populationK Rouault, V Scotet, S Autret, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|April 25, 2020
Penetrance is a critical parameter for assessing the disease liability of CFTR variantsA Boussaroque, M-P Audrézet, C Raynal, 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.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|May 21, 2005
[Neonatal screening of cystic fibrosis: diagnostic and ethical problems with mild mutations]M Roussey, A Le Bihannic, M P Audrezet, et al.
Journal of Inherited Metabolic Disease|July 17, 2007
Neonatal screening of cystic fibrosis: diagnostic problems with CFTR mild mutationsM Roussey, A Le Bihannic, V Scotet, et al.
Lancet (London, England)|October 7, 2000
Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosisV Scotet, M de Braekeleer, M Roussey, et al.
Pageof 2