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Blood Cells, Molecules & Diseases|May 10, 2003
Phenotypic expression of the C282Y/Q283P compound heterozygosity in HFE and molecular modeling of the Q283P mutation effectGérald Le Gac, François-Yves Dupradeau, Catherine Mura, et al.
Pediatrics|October 4, 2006
Immunoreactive trypsin/DNA newborn screening for cystic fibrosis: should the R117H variant be included in CFTR mutation panels?Virginie Scotet, Marie-Pierre Audrézet, Michel Roussey, et al.
BMC Medical Genetics|June 3, 2005
Impact of HFE genetic testing on clinical presentation of hereditary hemochromatosis: new epidemiological dataVirginie Scotet, Gérald Le Gac, Marie-Christine Mérour, et al.
BMC Pregnancy and Childbirth|February 19, 2018
Do pregnancies reduce iron overload in HFE hemochromatosis women? results from an observational prospective studyVirginie Scotet, Philippe Saliou, Marianne Uguen, et al.
Human Genetics|September 7, 2002
Spatial and temporal distribution of cystic fibrosis and of its mutations in Brittany, France: a retrospective study from 1960Virginie Scotet, Dominique Gillet, Ingrid Duguépéroux, et al.
Prenatal Diagnosis|November 5, 2011
Nonvisualization of fetal gallbladder increases the risk of cystic fibrosisIngrid Duguépéroux, Virginie Scotet, Marie-Pierre Audrézet, et al.
Pancreas|March 26, 2010
Genetic analysis of the glycoprotein 2 gene in patients with chronic pancreatitisEmmanuelle Masson, Sumit Paliwal, Seema Bhaskar, et al.
Endoscopy|May 21, 2016
Measures to improve microbial quality surveillance of gastrointestinal endoscopesPhilippe Saliou, Hervé Le Bars, Christopher Payan, et al.
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