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Human Genetics|April 17, 1998
Allele frequencies of hereditary hemochromatosis gene mutations in a local population of west BrittanyP Jézéquel, M Bargain, F Lellouche, et al.
Undersea & Hyperbaric Medicine : Journal of the Undersea and Hyperbaric Medical Society, Inc|July 5, 2011
Hemoptysis and pneumomediastinum after breath-hold diving in shallow water: a case reportA Henckes, J Arvieux, G Cochard, et al.
Annales De Biologie Clinique|June 26, 2004
[Manufacture of DNA chips in a laboratory for internal use: legislation and quality assurance]P Jézéquel, J Pichon, F Magrangeas, et al.
British Journal of Cancer|June 11, 2009
Validation of UBE2C protein as a prognostic marker in node-positive breast cancerD Loussouarn, L Campion, F Leclair, et al.
Human Mutation|January 1, 1995
French CF family genotype analysis shows that the R297Q mutation is a rare polymorphismI Dorval, P Jézéquel, B Chauvel, et al.
Molecular Human Reproduction|December 2, 2000
Molecular screening of the CFTR gene in men with anomalies of the vas deferens: identification of three novel mutationsP Jézéquel, C Dubourg, D Le Lannou, et al.
Clinical Chemistry|June 1, 1995
Structural analysis of CFTR gene in congenital bilateral absence of vas deferensP Jézéquel, I Dorval, P Fergelot, et al.
British Journal of Cancer|January 8, 2004
G388R mutation of the FGFR4 gene is not relevant to breast cancer prognosisP Jézéquel, L Campion, M-P Joalland, et al.
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