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Medical Principles and Practice : International Journal of the Kuwait University, Health Science Centre|October 3, 2018
Diet and Lifestyle Role in Homocysteine Metabolism in Turner SyndromeValeria Calcaterra, Daniela Larizza, Rachele De Giuseppe, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|November 12, 2017
Relation between circulating oxidized-LDL and metabolic syndrome in children with obesity: the role of hypertriglyceridemic waist phenotypeValeria Calcaterra, Rachele De Giuseppe, Ginevra Biino, et al.European Journal of Human Genetics : EJHG|May 26, 2006
Delineation of the ADULT syndrome phenotype due to arginine 298 mutations of the p63 geneTuula Rinne, Emanuela Spadoni, Klaus W Kjaer, et al.Diabetes|January 17, 2008
Variations of the perforin gene in patients with type 1 diabetesElisabetta Orilieri, Giuseppe Cappellano, Rita Clementi, et al.Human Molecular Genetics|April 27, 2017
A frequent oligogenic involvement in congenital hypothyroidismTiziana de Filippis, Giulia Gelmini, Elvezia Paraboschi, et al.The Journal of Clinical Endocrinology and Metabolism|November 8, 2016
Contribution of LHX4 Mutations to Pituitary Deficits in a Cohort of 417 Unrelated PatientsEnzo Cohen, Mohamad Maghnie, Nathalie Collot, et al.Human Mutation|October 14, 2005
Identification of sixty-two novel and twelve known FBN1 mutations in eighty-one unrelated probands with Marfan syndrome and other fibrillinopathiesEloisa Arbustini, Maurizia Grasso, Silvia Ansaldi, et al.Human Mutation|November 10, 2018
Small supernumerary marker chromosomes: A legacy of trisomy rescue?Nehir Edibe Kurtas, Luciano Xumerle, Lorena Leonardelli, et al.Pageof 5