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Human Genetics|August 25, 2007
Polymorphic length of FOXE1 alanine stretch: evidence for genetic susceptibility to thyroid dysgenesisAurore Carré, Mireille Castanet, Sylvia Sura-Trueba, et al.Alimentary Pharmacology & Therapeutics|February 5, 2022
Prevalence of HFE-related haemochromatosis and secondary causes of hyperferritinaemia and their association with iron overload in 1059 French patients treated by venesectionGérald Le Gac, Virginie Scotet, Isabelle Gourlaouen, et al.American Journal of Epidemiology|July 10, 2003
Hereditary hemochromatosis: effect of excessive alcohol consumption on disease expression in patients homozygous for the C282Y mutationVirginie Scotet, Marie-Christine Mérour, Anne-Yvonne Mercier, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|March 26, 2016
Highlighting the impact of cascade carrier testing in cystic fibrosis familiesIngrid Duguépéroux, Carine L'Hostis, Marie-Pierre Audrézet, et al.Human Mutation|June 20, 2003
Comparison of the CFTR mutation spectrum in three cohorts of patients of Celtic origin from Brittany (France) and IrelandVirginie Scotet, David E Barton, James B G Watson, et al.Plos One|December 17, 2013
Evidence for the high importance of co-morbid factors in HFE C282Y/H63D patients cared by phlebotomies: results from an observational prospective studyPhilippe Saliou, Gérald Le Gac, Anne-Yvonne Mercier, et al.Journal of Hepatology|December 3, 2014
Genome-wide association study identifies TF as a significant modifier gene of iron metabolism in HFE hemochromatosisMarie de Tayrac, Marie-Paule Roth, Anne-Marie Jouanolle, et al.Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 30, 2018
Primary sclerosing cholangitis is associated with abnormalities in CFTRSteven Werlin, Virginie Scotet, Kevin Uguen, et al.European Journal of Human Genetics : EJHG|November 13, 2004
A large-scale study of the random variability of a coding sequence: a study on the CFTR geneGuido Modiano, Cristina Bombieri, Bianca Maria Ciminelli, et al.Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]|December 14, 2022
The PRSS3P2 and TRY7 deletion copy number variant modifies risk for chronic pancreatitisEmmanuelle Masson, Maren Ewers, Sumit Paliwal, et al.Pageof 4