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L Tranebjaerg

Showing results (21-30 of 107) with videos related to

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Clinical Genetics|February 9, 2000
Proximal myotonic myopathy: clinical and molecular investigation of a Norwegian family with PROMMC Sun, O A Henriksen, L Tranebjaerg
Advances in Oto-Rhino-Laryngology|June 27, 2000
DFNA7L Tranebjaerg, H H Elverland, T Fagerheim
Nephron|January 1, 1985
Plasma antithrombin III concentration in patients on regular haemodialysis treatmentM Jørgensen, H O Eriksen, L Tranebjaerg
Scandinavian Journal of Urology and Nephrology|January 1, 1983
Parathyroidectomy for hyperparathyroidism in maintenance dialysis patientsJ G Heaf, L Tranebjaerg, H Wolf
Advances in Oto-Rhino-Laryngology|June 27, 2000
X-linked recessive deafness-dystonia syndrome (Mohr-Tranebjaerg syndrome)L Tranebjaerg, P K Jensen, M van Ghelue
Scandinavian 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.
Cardiovascular 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.
Acta Ophthalmologica Scandinavica|December 1, 1996
Full-field electroretinograms in a family with Mohr-Tranebjaerg syndromeV Ponjavic, S Andreasson, L Tranebjaerg, et al.
Pageof 11

Showing results (21-30 of 107) with videos related to

Sort By:
Pageof 11
Clinical Genetics|February 9, 2000
Proximal myotonic myopathy: clinical and molecular investigation of a Norwegian family with PROMMC Sun, O A Henriksen, L Tranebjaerg
Advances in Oto-Rhino-Laryngology|June 27, 2000
DFNA7L Tranebjaerg, H H Elverland, T Fagerheim
Nephron|January 1, 1985
Plasma antithrombin III concentration in patients on regular haemodialysis treatmentM Jørgensen, H O Eriksen, L Tranebjaerg
Scandinavian Journal of Urology and Nephrology|January 1, 1983
Parathyroidectomy for hyperparathyroidism in maintenance dialysis patientsJ G Heaf, L Tranebjaerg, H Wolf
Advances in Oto-Rhino-Laryngology|June 27, 2000
X-linked recessive deafness-dystonia syndrome (Mohr-Tranebjaerg syndrome)L Tranebjaerg, P K Jensen, M van Ghelue
Scandinavian 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.
Cardiovascular 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.
Acta Ophthalmologica Scandinavica|December 1, 1996
Full-field electroretinograms in a family with Mohr-Tranebjaerg syndromeV Ponjavic, S Andreasson, L Tranebjaerg, et al.
Pageof 11