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L Tranebjaerg

Showing results (41-50 of 107) with videos related to

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American Journal of Medical Genetics|April 1, 1988
Interstitial deletion 13q: further delineation of the syndrome by clinical and high-resolution chromosome analysis of five patientsL Tranebjaerg, K B Nielsen, N Tommerup, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|December 1, 1983
Plasma fibronectin concentration in patients with chronic renal failure and treated with haemodialysisH O Eriksen, L Tranebjaerg, I Clemmensen, et al.
American Journal of Medical Genetics|July 15, 1994
Prevalence of fra(X) in the county of Funen in Denmark is lower than expectedL Tranebjaerg, S Hilling, J Jessen, et al.
Journal of Medical Genetics|February 1, 1987
New assignment of the adenosine deaminase gene locus to chromosome 20q13 X 11 by study of a patient with interstitial deletion 20qM B Petersen, L Tranebjaerg, N Tommerup, et al.
American Journal of Medical Genetics|April 20, 1999
XLMR genes: update 1998H Lubs, P Chiurazzi, J Arena, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|July 1, 1999
[X-linked recessive bulbospinal neuronopathy--Kennedy's syndrome]K V Andersen, R P Michler, O Nilssen, et al.
Ugeskrift for Laeger|October 17, 1988
[Abdominal symptoms as the first sign in Schönlein-Henoch syndrome]P Albertsen, S Petersen, B Pilgaard, et al.
American Journal of Human Genetics|March 3, 1999
Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivationR M Plenge, L Tranebjaerg, P K Jensen, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|April 1, 1984
Plasma and urine fibronectin concentration in kidney-transplanted patientsH O Eriksen, O Skjoldby, H Kjersem, et al.
Acta Obstetricia Et Gynecologica Scandinavica|April 1, 1995
Prenatal diagnosis of osteogenesis imperfectaL N Berge, V Marton, L Tranebjaerg, et al.
Pageof 11

Showing results (41-50 of 107) with videos related to

Sort By:
Pageof 11
American Journal of Medical Genetics|April 1, 1988
Interstitial deletion 13q: further delineation of the syndrome by clinical and high-resolution chromosome analysis of five patientsL Tranebjaerg, K B Nielsen, N Tommerup, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|December 1, 1983
Plasma fibronectin concentration in patients with chronic renal failure and treated with haemodialysisH O Eriksen, L Tranebjaerg, I Clemmensen, et al.
American Journal of Medical Genetics|July 15, 1994
Prevalence of fra(X) in the county of Funen in Denmark is lower than expectedL Tranebjaerg, S Hilling, J Jessen, et al.
Journal of Medical Genetics|February 1, 1987
New assignment of the adenosine deaminase gene locus to chromosome 20q13 X 11 by study of a patient with interstitial deletion 20qM B Petersen, L Tranebjaerg, N Tommerup, et al.
American Journal of Medical Genetics|April 20, 1999
XLMR genes: update 1998H Lubs, P Chiurazzi, J Arena, et al.
Tidsskrift for Den Norske Laegeforening : Tidsskrift for Praktisk Medicin, Ny Raekke|July 1, 1999
[X-linked recessive bulbospinal neuronopathy--Kennedy's syndrome]K V Andersen, R P Michler, O Nilssen, et al.
Ugeskrift for Laeger|October 17, 1988
[Abdominal symptoms as the first sign in Schönlein-Henoch syndrome]P Albertsen, S Petersen, B Pilgaard, et al.
American Journal of Human Genetics|March 3, 1999
Evidence that mutations in the X-linked DDP gene cause incompletely penetrant and variable skewed X inactivationR M Plenge, L Tranebjaerg, P K Jensen, et al.
Scandinavian Journal of Clinical and Laboratory Investigation|April 1, 1984
Plasma and urine fibronectin concentration in kidney-transplanted patientsH O Eriksen, O Skjoldby, H Kjersem, et al.
Acta Obstetricia Et Gynecologica Scandinavica|April 1, 1995
Prenatal diagnosis of osteogenesis imperfectaL N Berge, V Marton, L Tranebjaerg, et al.
Pageof 11