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C Cazeneuve

Showing results (11-20 of 41) with videos related to

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Human Heredity|January 1, 1995
Identification of a novel missense mutation G239R in exon 6a of the CFTR geneT Bienvenu, C Cazeneuve, I Fajac, et al.
Revue Neurologique|June 6, 2017
Motor neuron disease of very long disease duration or Charcot-Marie-Tooth disease? A novel phenotype related to the SOD1 p.E22G variantG Querin, P Corcia, T Lenglet, et al.
Soft Matter|February 17, 2015
Surfactant-polymer interactions: molecular architecture does matterS Banerjee, C Cazeneuve, N Baghdadli, et al.
Human Molecular Genetics|December 15, 2000
Alternative splicing at the MEFV locus involved in familial Mediterranean fever regulates translocation of the marenostrin/pyrin protein to the nucleusS Papin, P Duquesnoy, C Cazeneuve, et al.
Human Genetics|June 1, 1995
Three novel sequence variations in the 5' upstream region of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: two polymorphisms and one putative molecular defectT Bienvenu, V Lacronique, M Raymondjean, et al.
Neurology|October 15, 2008
Re: Alpha-synuclein gene duplication is present in sporadic Parkinson diseaseA R Troiano, C Cazeneuve, I Le Ber, et al.
Clinical Chemistry|June 13, 1998
Clinical evaluation of the CF(12)m cystic fibrosis DNA diagnostic kitC Houdayer, C Cazeneuve, E Cougoureux, et al.
Arthritis and Rheumatism|October 29, 2005
MEFV analysis is of particularly weak diagnostic value for recurrent fevers in Western European Caucasian patientsD Tchernitchko, S Moutereau, M Legendre, et al.
Hepatology (Baltimore, Md.)|January 13, 1998
Hemochromatosis Cys282Tyr mutation and liver iron overload in patients with chronic active hepatitis CC Hezode, C Cazeneuve, O Coué, et al.
Human Mutation|September 8, 1999
A noval nonsense mutation (Y849X) in the CFTR gene of a CF patient from southern ItalyG Castaldo, A Fuccio, C Cazeneuve, et al.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
Human Heredity|January 1, 1995
Identification of a novel missense mutation G239R in exon 6a of the CFTR geneT Bienvenu, C Cazeneuve, I Fajac, et al.
Revue Neurologique|June 6, 2017
Motor neuron disease of very long disease duration or Charcot-Marie-Tooth disease? A novel phenotype related to the SOD1 p.E22G variantG Querin, P Corcia, T Lenglet, et al.
Soft Matter|February 17, 2015
Surfactant-polymer interactions: molecular architecture does matterS Banerjee, C Cazeneuve, N Baghdadli, et al.
Human Molecular Genetics|December 15, 2000
Alternative splicing at the MEFV locus involved in familial Mediterranean fever regulates translocation of the marenostrin/pyrin protein to the nucleusS Papin, P Duquesnoy, C Cazeneuve, et al.
Human Genetics|June 1, 1995
Three novel sequence variations in the 5' upstream region of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: two polymorphisms and one putative molecular defectT Bienvenu, V Lacronique, M Raymondjean, et al.
Neurology|October 15, 2008
Re: Alpha-synuclein gene duplication is present in sporadic Parkinson diseaseA R Troiano, C Cazeneuve, I Le Ber, et al.
Clinical Chemistry|June 13, 1998
Clinical evaluation of the CF(12)m cystic fibrosis DNA diagnostic kitC Houdayer, C Cazeneuve, E Cougoureux, et al.
Arthritis and Rheumatism|October 29, 2005
MEFV analysis is of particularly weak diagnostic value for recurrent fevers in Western European Caucasian patientsD Tchernitchko, S Moutereau, M Legendre, et al.
Hepatology (Baltimore, Md.)|January 13, 1998
Hemochromatosis Cys282Tyr mutation and liver iron overload in patients with chronic active hepatitis CC Hezode, C Cazeneuve, O Coué, et al.
Human Mutation|September 8, 1999
A noval nonsense mutation (Y849X) in the CFTR gene of a CF patient from southern ItalyG Castaldo, A Fuccio, C Cazeneuve, et al.
Pageof 5