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European Journal of Human Genetics : EJHG|August 22, 2000
Linkage disequilibrium in inbred North African families allows fine genetic and physical mapping of triple A syndromeS Hadj-Rabia, R Salomon, A Pelet, et al.Annales De Dermatologie Et De Venereologie|June 30, 2005
[How should severe and chronic atopic dermatitis in children be managed?]C BodemerArchives of Dermatology|August 1, 1982
Dinitrochlorobenzene treatment of alopecia areataY de Prost, F Paquez, R TouraineEuropean Journal of Human Genetics : EJHG|July 1, 1997
Three novel point mutations in the keratinocyte transglutaminase (TGK) gene in lamellar ichthyosis: significance for mutant transcript level, TGK immunodetection and activityE Petit, M Huber, A Rochat, et al.American Journal of Human Genetics|October 27, 1997
Characterization of 18 new mutations in COL7A1 in recessive dystrophic epidermolysis bullosa provides evidence for distinct molecular mechanisms underlying defective anchoring fibril formationA Hovnanian, A Rochat, C Bodemer, et al.Annales De Dermatologie Et De Venereologie|July 4, 2021
Development and co-construction of a therapeutic patient education program for albinismH Dufresne, A de Longcamp, S Compain, et al.The British Journal of Dermatology|November 4, 2014
Psoriasis and obesity in French children: a case-control, multicentre studyE Mahé, A Beauchet, C Bodemer, et al.Human Mutation|October 26, 1999
Protein truncation test for screening hamartin gene mutations and report of new disease-causing mutationsP Bénit, A Kara-Mostefa, S Hadj-Rabia, et al.Pageof 38