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C Ferec

Showing results (61-70 of 103) with videos related to

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Molecular Genetics and Metabolism|November 16, 2001
Identification of a novel pancreatitis-associated missense mutation, R116C, in the human cationic trypsinogen gene (PRSS1)C Le Maréchal, J F Bretagne, O Raguénès, et al.
Gastroenterology|December 28, 1999
The A16V signal peptide cleavage site mutation in the cationic trypsinogen gene and chronic pancreatitisJ M Chen, O Raguenes, C Ferec, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Novel mutations in the duplicated region of PKD1 geneR Perrichot, B Mercier, I Quere, et al.
Archives Francaises De Pediatrie|May 1, 1988
[Molecular biology and mucoviscidosis. Brest experience in 1987]P Parent, C Ferec, M Jehanne, et al.
Human Genetics|January 24, 1998
Phenotype-genotype correlation in haemochromatosis subjectsC Mura, J B Nousbaum, P Verger, et al.
Journal of Medical Genetics|May 1, 1993
Mild pulmonary, but severe hepatic disease in a cystic fibrosis patient homozygous for a frameshift mutation in the regulatory domain of the CFTRW Lissens, S Desmyttere, M Bonduelle, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|February 1, 1984
[Serological profile in so-called seronegative rheumatoid arthritis]M P Moineau, P Youinou, P Le Goff, et al.
Collegium Antropologicum|February 24, 2001
Microsatellite haplotypes associations with 5 CFTR mutations in "Grande Brière", an isolate located in southern BrittanyS Bezieau, G Picherot, A David, et al.
Digestive Diseases and Sciences|July 1, 1996
An exceptional genealogy for hereditary chronic pancreatitisL Le Bodic, M Schnee, T Georgelin, et al.
Biochemical and Biophysical Research Communications|October 29, 1998
New biocompatible cationic amphiphiles derivative from glycine betaine: a novel family of efficient nonviral gene transfer agentsV Floch, N Legros, S Loisel, et al.
Pageof 11

Showing results (61-70 of 103) with videos related to

Sort By:
Pageof 11
Molecular Genetics and Metabolism|November 16, 2001
Identification of a novel pancreatitis-associated missense mutation, R116C, in the human cationic trypsinogen gene (PRSS1)C Le Maréchal, J F Bretagne, O Raguénès, et al.
Gastroenterology|December 28, 1999
The A16V signal peptide cleavage site mutation in the cationic trypsinogen gene and chronic pancreatitisJ M Chen, O Raguenes, C Ferec, et al.
European Journal of Human Genetics : EJHG|June 15, 2000
Novel mutations in the duplicated region of PKD1 geneR Perrichot, B Mercier, I Quere, et al.
Archives Francaises De Pediatrie|May 1, 1988
[Molecular biology and mucoviscidosis. Brest experience in 1987]P Parent, C Ferec, M Jehanne, et al.
Human Genetics|January 24, 1998
Phenotype-genotype correlation in haemochromatosis subjectsC Mura, J B Nousbaum, P Verger, et al.
Journal of Medical Genetics|May 1, 1993
Mild pulmonary, but severe hepatic disease in a cystic fibrosis patient homozygous for a frameshift mutation in the regulatory domain of the CFTRW Lissens, S Desmyttere, M Bonduelle, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|February 1, 1984
[Serological profile in so-called seronegative rheumatoid arthritis]M P Moineau, P Youinou, P Le Goff, et al.
Collegium Antropologicum|February 24, 2001
Microsatellite haplotypes associations with 5 CFTR mutations in "Grande Brière", an isolate located in southern BrittanyS Bezieau, G Picherot, A David, et al.
Digestive Diseases and Sciences|July 1, 1996
An exceptional genealogy for hereditary chronic pancreatitisL Le Bodic, M Schnee, T Georgelin, et al.
Biochemical and Biophysical Research Communications|October 29, 1998
New biocompatible cationic amphiphiles derivative from glycine betaine: a novel family of efficient nonviral gene transfer agentsV Floch, N Legros, S Loisel, et al.
Pageof 11