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P Freisinger

Showing results (1-10 of 31) with videos related to

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American Journal of Medical Genetics|January 15, 1993
Collagen fibrils of osteoid in osteogenesis imperfecta: morphometrical analysis of the fibril diameterH Stöss, P Freisinger
Der Pathologe|March 1, 1993
[Osteogenesis imperfecta with hyperplastic callus formation]H Stöss, P Freisinger
Skeletal Radiology|March 21, 1998
Severe rhizomelic skeletal dysplasia in a museum skeletonA G Nerlich, P Freisinger
American Journal of Medical Genetics|February 15, 1993
DysspondylochondromatosisP Freisinger, G Finidori, P Maroteaux
The Journal of Bone and Joint Surgery. British Volume|September 1, 1991
Pachydysostosis of the fibulaP Maroteaux, P Freisinger, M Le Merrer
American Journal of Medical Genetics|May 3, 1996
Radiological and histological variants of thanatophoric dysplasia are associated with common mutations in FGFR-3A G Nerlich, P Freisinger, J Bonaventure
Journal of Medical Genetics|November 1, 1992
An atypical form of mucolipidosis IIIP Freisinger, J C Padovani, P Maroteaux
Journal of Medical Genetics|August 1, 1993
Dominant carpotarsal osteochondromatosisP Maroteaux, M Le Merrer, H Bensahel, et al.
Journal of Inherited Metabolic Disease|February 19, 2004
Reversion of hypertrophic cardiomyopathy in a patient with deficiency of the mitochondrial copper binding protein Sco2: is there a potential effect of copper?P Freisinger, R Horvath, C Macmillan, et al.
Journal of Inherited Metabolic Disease|March 21, 1998
Symptomatic ornithine carbamoyltransferase deficiency (point mutation H202P) with normal in vitro activityM Staudt, B Wermuth, P Freisinger, et al.
Pageof 4

Showing results (1-10 of 31) with videos related to

Sort By:
Pageof 4
American Journal of Medical Genetics|January 15, 1993
Collagen fibrils of osteoid in osteogenesis imperfecta: morphometrical analysis of the fibril diameterH Stöss, P Freisinger
Der Pathologe|March 1, 1993
[Osteogenesis imperfecta with hyperplastic callus formation]H Stöss, P Freisinger
Skeletal Radiology|March 21, 1998
Severe rhizomelic skeletal dysplasia in a museum skeletonA G Nerlich, P Freisinger
American Journal of Medical Genetics|February 15, 1993
DysspondylochondromatosisP Freisinger, G Finidori, P Maroteaux
The Journal of Bone and Joint Surgery. British Volume|September 1, 1991
Pachydysostosis of the fibulaP Maroteaux, P Freisinger, M Le Merrer
American Journal of Medical Genetics|May 3, 1996
Radiological and histological variants of thanatophoric dysplasia are associated with common mutations in FGFR-3A G Nerlich, P Freisinger, J Bonaventure
Journal of Medical Genetics|November 1, 1992
An atypical form of mucolipidosis IIIP Freisinger, J C Padovani, P Maroteaux
Journal of Medical Genetics|August 1, 1993
Dominant carpotarsal osteochondromatosisP Maroteaux, M Le Merrer, H Bensahel, et al.
Journal of Inherited Metabolic Disease|February 19, 2004
Reversion of hypertrophic cardiomyopathy in a patient with deficiency of the mitochondrial copper binding protein Sco2: is there a potential effect of copper?P Freisinger, R Horvath, C Macmillan, et al.
Journal of Inherited Metabolic Disease|March 21, 1998
Symptomatic ornithine carbamoyltransferase deficiency (point mutation H202P) with normal in vitro activityM Staudt, B Wermuth, P Freisinger, et al.
Pageof 4