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Ugeskrift for Laeger|June 27, 2000
[Child abuse and osteogenesis imperfecta. How do we distinguish?]A M Lund, F Skovby, F U KnudsenEuropean Journal of Pediatrics|October 1, 1991
Optic gliomas in children with neurofibromatosis type 1A M Lund, F SkovbyClinical Genetics|November 1, 1996
Variable clinical expression in a family with OI type IV due to deletion of three base pairs in COL1A1A M Lund, M Schwartz, F SkovbyPrenatal Diagnosis|November 1, 1996
Genetic counselling and prenatal diagnosis of osteogenesis imperfecta caused by paternal mosaicismA M Lund, M Schwartz, F SkovbyHuman Genetics|March 1, 1996
Deletion of a Gly-Pro-Pro repeat in the pro alpha2(I) chain of procollagen I in a family with dominant osteogenesis imperfecta type IVA M Lund, F Skovby, M SchwartzArchives of Disease in Childhood|May 20, 1999
Anthropometry of patients with osteogenesis imperfectaA M Lund, J Müller, F SkovbyHuman Mutation|January 1, 1997
(G586V) substitutions in the alpha 1 and alpha 2 chains of collagen I: effect of alpha-chain stoichiometry on the phenotype of osteogenesis imperfecta?A M Lund, F Skovby, M SchwartzActa Paediatrica (Oslo, Norway : 1992)|November 24, 1999
Bone mineral content and collagen defects in osteogenesis imperfectaA M Lund, C Mølgaard, J Müller, et al.Pageof 16