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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 KnudsenHuman Genetics|July 1, 1995
Assignment of congenital cataract Volkmann type (CCV) to chromosome 1p36H Eiberg, A M Lund, M Warburg, et al.Nephron|September 8, 1998
Atraumatic loss of a kidney in a patient with alpha1-antitrypsin deficiencyE Randers, M Jønler, A M Lund, et al.Acta Paediatrica (Oslo, Norway : 1992)|November 24, 1999
Bone mineral content and collagen defects in osteogenesis imperfectaA M Lund, C Mølgaard, J Müller, et al.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.Pageof 6