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Journal of Hepatology|March 1, 1991
Short-term prednisolone followed by recombinant human alpha-interferon alone or combined with adenine-arabinoside in chronic hepatitis B. A prospective and randomized trialP Brissot, C Jacquelinet, H Jouanolle, 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.Human Reproduction (Oxford, England)|February 1, 1995
Obstructive azoospermia with agenesis of vas deferens or with bronchiectasia (Young's syndrome): a genetic approachD Le Lannou, P Jezequel, M Blayau, et al.Human Genetics|January 1, 1989
Ferritin H gene polymorphism in idiopathic hemochromatosisV David, P Papadopoulos, J Yaouanq, et al.European Journal of Gastroenterology & Hepatology|July 4, 2001
A new mutation of E-cadherin gene in familial gastric linitis plastica cancer with extra-digestive disseminationL Dussaulx-Garin, M Blayau, M Pagenault, et al.American Journal of Human Genetics|February 1, 1994
Anonymous marker loci within 400 kb of HLA-A generate haplotypes in linkage disequilibrium with the hemochromatosis gene (HFE)J Yaouanq, M Perichon, M Chorney, et al.Human Genetics|April 1, 1992
Anonymous markers located on chromosome 6 in the HLA-A class I region: allelic distribution in genetic haemochromatosisJ Boretto, A M Jouanolle, J Yaouanq, et al.Journal of Medical Genetics|May 1, 1992
Familial screening for genetic haemochromatosis by means of DNA markersJ Yaouanq, A el Kahloun, M Chorney, et al.Bulletin De L'Academie Nationale De Medecine|February 1, 1993
[Molecular genetics of hemochromatosis]J Y Le Gall, V David, J Yaouanq, et al.Pageof 3