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American Journal of Medical Genetics. Supplement|January 1, 1990
Clinical, cytogenetic, and molecular genetic characterization of two unrelated patients with different duplications of 21qM B Petersen, L Tranebjaerg, M K McCormick, et al.Acta Paediatrica Scandinavica|November 1, 1991
Immunoglobulin and complement studies in children with Schönlein-Henoch Syndrome and other vasculitic diseasesS Petersen, E Taaning, T Söderström, et al.Journal of Medical Genetics|May 2, 2006
Autosomal dominant optic atrophy associated with hearing impairment and impaired glucose regulation caused by a missense mutation in the WFS1 geneH Eiberg, L Hansen, B Kjer, et al.Human Molecular Genetics|January 1, 1997
Quantification, by solid-phase minisequencing, of the telomeric and centromeric copies of the survival motor neuron gene in families with spinal muscular atrophyM Schwartz, N Sørensen, F J Hansen, et al.Journal of Perinatology : Official Journal of the California Perinatal Association|July 16, 2011
A practical guide to neonatal volume guarantee ventilationC Klingenberg, K I Wheeler, P G Davis, et al.Scandinavian Journal of Infectious Diseases|August 23, 2001
Rapid detection of the methicillin-resistance gene, mecA, in coagulase-negative StaphylococciT Glad, C Klingenberg, T Flaegstad, et al.Prenatal Diagnosis|February 1, 1994
Early prenatal direct gene diagnosis of cystic fibrosis in a twin pregnancy and subsequent selective terminationF S Jørgensen, J Bang, L Tranebjaerg, et al.Human Genetics|February 1, 1994
394delTT: a Nordic cystic fibrosis mutationM Schwartz, M Anvret, M Claustres, et al.American Journal of Human Genetics|January 23, 1999
Spectrum of mutations in alpha-mannosidosisT Berg, H M Riise, G M Hansen, et al.Clinical and Experimental Dermatology|September 18, 2010
A novel mutation in the connexin 26 gene (GJB2) in a child with clinical and histological features of keratitis-ichthyosis-deafness (KID) syndromeU Koppelhus, L Tranebjaerg, G Esberg, et al.Pageof 11