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Ugeskrift for Laeger|July 8, 1991
[The Angelman syndrome. Does the phenotype depend on maternal inheritance?]A M LundEuropean Journal of Pediatrics|October 1, 1991
Optic gliomas in children with neurofibromatosis type 1A M Lund, F SkovbyArchives of Disease in Childhood|November 24, 2001
Feeding difficulties in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyA M Lund, J V LeonardJournal of Craniofacial Genetics and Developmental Biology|July 1, 1997
Osteogenesis imperfecta: clinical, cephalometric, and biochemical investigations of OI types I, III, and IVB L Jensen, A M LundHuman 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 SchwartzClinical 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 SkovbyArchives 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 SchwartzPageof 6