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Ophthalmic Paediatrics and Genetics|December 1, 1986
Retinal cone dysfunction and mental retardation associated with a de novo balanced translocation 1;6(q44;q27)L Tranebjaerg, O Sjø, M WarburgChromosoma|January 23, 1999
A neocentromere on human chromosome 3 without detectable alpha-satellite DNA forms morphologically normal kinetochoresA Wandall, L Tranebjaerg, N TommerupClinical Genetics|February 9, 2000
Proximal myotonic myopathy: clinical and molecular investigation of a Norwegian family with PROMMC Sun, O A Henriksen, L TranebjaergNephron|January 1, 1985
Plasma antithrombin III concentration in patients on regular haemodialysis treatmentM Jørgensen, H O Eriksen, L TranebjaergScandinavian Journal of Urology and Nephrology|January 1, 1983
Parathyroidectomy for hyperparathyroidism in maintenance dialysis patientsJ G Heaf, L Tranebjaerg, H WolfScandinavian Audiology|February 16, 2002
Two families with phenotypically different hereditary low frequency hearing impairment: longitudinal data and linkage analysisM Bille, L Munk-Nielsen, L Tranebjaerg, et al.Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|November 10, 1993
[Retroperitoneal chylous cyst]C Klingenberg, T E JohansenCardiovascular Research|September 1, 2001
A spectrum of functional effects for disease causing mutations in the Jervell and Lange-Nielsen syndromeL Huang, M Bitner-Glindzicz, L Tranebjaerg, et al.Journal of Medical Genetics|May 1, 1994
Aspartylglucosaminuria in northern Norway: a molecular and genealogical studyO K Tollersrud, O Nilssen, L Tranebjaerg, et al.American Journal of Medical Genetics|June 1, 1991
Deletion mapping of a retinal cone-rod dystrophy: assignment to 18q211M Warburg, O Sjö, L Tranebjaerg, et al.Pageof 11