Showing results (31-40 of 435) with videos related to
Sort By:
Pageof 44
Human Genetics|January 1, 1989
Ferritin H gene polymorphism in idiopathic hemochromatosisV David, P Papadopoulos, J Yaouanq, et al.Journal of Medical Genetics|November 13, 2007
Impairment of CDKL5 nuclear localisation as a cause for severe infantile encephalopathyH Rosas-Vargas, N Bahi-Buisson, C Philippe, 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.Diabetes & Metabolism|November 21, 2002
Serum paraoxonase activity and paraoxonase gene polymorphism in type 2 diabetic patients with or without vascular complicationsC Letellier, M R Durou, A M Jouanolle, et al.Genetic Counseling (Geneva, Switzerland)|January 1, 1990
Triphalangeal thumb and split foot in the same familyB Le Marec, S Odent, C TreguierGeriatrics|September 1, 1994
Low back pain: how to make the diagnosis in the older patientL Lazaro, R J QuinetJournal 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.Archives of Andrology|January 1, 1988
Alpha-L-fucosidase in rat testis during sexual maturityG Leray, V Shacoori, C Prodhomme, et al.Annales De Gastroenterologie Et D'Hepatologie|November 1, 1993
[Molecular genetics of hemochromatosis]J Y Le Gall, V David, J Yaouanq, et al.Pageof 44