Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Vox Sanguinis|July 22, 2016
The experience of extended blood group genotyping by next-generation sequencing (NGS): investigation of patients with sickle-cell diseaseY Fichou, M Mariez, C Le Maréchal, et al.
Cytogenetic and Genome Research|March 17, 2009
Copy number variations in chronic pancreatitisJ M Chen, E Masson, C Le Maréchal, et al.
Physiological Reports|July 22, 2024
Association between rat decompression sickness resistance, transthyretin single nucleotide polymorphism, and expression: A pilot studyJ Orsat, A Guernec, C Le Maréchal, et al.
Human Genetics|May 31, 2001
Complete and rapid scanning of the cystic fibrosis transmembrane conductance regulator (CFTR) gene by denaturing high-performance liquid chromatography (D-HPLC): major implications for genetic counsellingC Le Maréchal, M P Audrézet, I Quéré, et al.
BMC Genetics|December 6, 2001
Discrimination of three mutational events that result in a disruption of the R122 primary autolysis site of the human cationic trypsinogen (PRSS1) by denaturing high performance liquid chromatographyC Le Maréchal, J M Chen, I Quéré, et al.
Veterinary Microbiology|September 11, 2017
A bovine botulism outbreak associated with a suspected cross-contamination from a poultry farmR Souillard, C Le Maréchal, V Ballan, et al.
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.
Journal of Microbiological Methods|September 9, 2009
Development of serological proteome analysis of mastitis by Staphylococcus aureus in ewesC Le Maréchal, G Jan, S Even, et al.
Acta Neurologica Scandinavica|May 12, 2018
Exercise testing-based algorithms to diagnose McArdle disease and MAD defectsJ-B Noury, F Zagnoli, J-L Carré, et al.
Human Mutation|January 15, 2004
Two novel severe mutations in the pancreatic secretory trypsin inhibitor gene (SPINK1) cause familial and/or hereditary pancreatitisC Le Maréchal, J M Chen, C Le Gall, et al.
Pageof 2