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La Nouvelle Presse Medicale|October 8, 1977
[HLA markers and periodic disease [familial Mediterranean fever (F.M.F.)] (author's transl)]Y Chaouat, J P Tormen, P Godeau, et al.
Prenatal Diagnosis|July 12, 2011
Diagnosis of fetal urinary tract malformations: prenatal management and postnatal outcomeA Ryckewaert-D'Halluin, G Le Bouar, S Odent, et al.
Molecular Genetics and Metabolism Reports|April 17, 2025
The recurrent p.Glu3Lys variant in EHHADH is responsible for Fanconi syndrome with early liver dysfunction and mitochondrial abnormalitiesP Rollier, A Cospain, M Barth, et al.
The Journal of Clinical Endocrinology and Metabolism|July 28, 2015
CYP24A1 Mutations in a Cohort of Hypercalcemic Patients: Evidence for a Recessive TraitA Molin, R Baudoin, M Kaufmann, et al.
Revue Du Rhumatisme Et Des Maladies Osteo-Articulaires|January 1, 1983
[Bone and phosphoro-calcium metabolism in reflex sympathetic dystrophy]J C Renier, M Basle, J Arlet, et al.
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