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Clinical Genetics|February 1, 1992
Autosomal dominant congenital cataract; linkage relations; clinical and genetic heterogeneityA M Lund, H Eiberg, T Rosenberg, et al.Journal of Food Protection|May 5, 2019
Comparison of Methods for Isolation of Listeria from Raw MilkA M Lund, E A Zottola, D J PuschScandinavian Journal of Clinical and Laboratory Investigation. Supplementum|January 1, 1986
On the mechanism of biosynthesis of cholestanol from 7 alpha-hydroxycholesterolM S Buchmann, I Björkhem, A M Lund, et al.Alcohol (Fayetteville, N.Y.)|August 18, 2000
Metabolism of some radiolabeled essential fatty acids in isolated rat hepatocytes is affected by dietary ethanolK Retterstøl, A M Lund, S Tverdal, et al.Acta Paediatrica (Oslo, Norway : 1992)|July 1, 1997
Parental mosaicism and autosomal dominant mutations causing structural abnormalities of collagen I are frequent in families with osteogenesis imperfecta type III/IVA M Lund, A C Nicholls, M Schwartz, et al.Journal of Inherited Metabolic Disease|March 6, 2007
Xanthurenic aciduria due to a mutation in KYNU encoding kynureninaseM Christensen, M Duno, A M Lund, et al.European Journal of Human Genetics : EJHG|January 1, 1996
Gly802Asp substitution in the pro alpha 2(I) collagen chain in a family with recurrent osteogenesis imperfecta due to paternal mosaicismA M Lund, M Schwartz, M Raghunath, et al.Journal of Endocrinological Investigation|September 4, 1999
Co-existence of osteogenesis imperfecta and hyperparathyroidismT Zimmermann-Belsing, A M Lund, L Christensen, et al.Human Genetics|June 1, 1993
SSCP detection of a Gly565Val substitution in the pro alpha 1(I) collagen chain resulting in osteogenesis imperfecta type IIK Mackay, A M Lund, M Raghunath, et al.Journal of Craniofacial Genetics and Developmental Biology|May 22, 1998
Dental manifestations of osteogenesis imperfecta and abnormalities of collagen I metabolismA M Lund, B L Jensen, L A Nielsen, et al.Pageof 13