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J Spranger

Showing results (161-170 of 247) with videos related to

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Human Mutation|January 1, 1994
Autosomal dominant spondylarthropathy due to a type II procollagen gene (COL2A1) point mutationA Winterpacht, M Hilbert, U Schwarze, et al.
American Journal of Medical Genetics|January 15, 1993
Osteogenesis imperfecta and hyperplastic callus formation: light- and electron-microscopic findingsH Stöss, B Pontz, U Vetter, et al.
Acta Paediatrica Belgica|April 1, 1977
Severe neonatal dwarfism resembling the Kniest and Rolland types of chondrodysplasiaJ P Farriaux, J Remy, G B Harris, et al.
Human Genetics|December 1, 1986
Severe short-limb dwarfism resembling Grebe chondrodysplasiaA S Teebi, S A Al-Awadi, J M Opitz, et al.
American Journal of Medical Genetics|November 1, 1984
Geleophysic dysplasiaJ Spranger, E F Gilbert, S Arya, et al.
Diabetologia|December 29, 2000
Release of the angiogenesis inhibitor angiostatin in patients with proliferative diabetic retinopathy: association with retinal photocoagulationJ Spranger, H P Hammes, K T Preissner, et al.
Human Genetics|December 18, 1998
Pigmentary mosaicism in hypomelanosis of Ito. Further evidence for functional disomy of XpB Fritz, W Küster, K H Orstavik, et al.
American Journal of Medical Genetics|May 3, 1996
Clinical and ultrastructural findings in three patients with geleophysic dysplasiaB F Pontz, H Stöss, F Henschke, et al.
Klinische Wochenschrift|October 1, 1974
A constitutional disorder of connective tissue suggesting a defect in collagen biosynthesisW N Meigel, P K Müller, B F Pontz, et al.
Nature Genetics|April 1, 1993
Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defectA Winterpacht, M Hilbert, U Schwarze, et al.
Pageof 25

Showing results (161-170 of 247) with videos related to

Sort By:
Pageof 25
Human Mutation|January 1, 1994
Autosomal dominant spondylarthropathy due to a type II procollagen gene (COL2A1) point mutationA Winterpacht, M Hilbert, U Schwarze, et al.
American Journal of Medical Genetics|January 15, 1993
Osteogenesis imperfecta and hyperplastic callus formation: light- and electron-microscopic findingsH Stöss, B Pontz, U Vetter, et al.
Acta Paediatrica Belgica|April 1, 1977
Severe neonatal dwarfism resembling the Kniest and Rolland types of chondrodysplasiaJ P Farriaux, J Remy, G B Harris, et al.
Human Genetics|December 1, 1986
Severe short-limb dwarfism resembling Grebe chondrodysplasiaA S Teebi, S A Al-Awadi, J M Opitz, et al.
American Journal of Medical Genetics|November 1, 1984
Geleophysic dysplasiaJ Spranger, E F Gilbert, S Arya, et al.
Diabetologia|December 29, 2000
Release of the angiogenesis inhibitor angiostatin in patients with proliferative diabetic retinopathy: association with retinal photocoagulationJ Spranger, H P Hammes, K T Preissner, et al.
Human Genetics|December 18, 1998
Pigmentary mosaicism in hypomelanosis of Ito. Further evidence for functional disomy of XpB Fritz, W Küster, K H Orstavik, et al.
American Journal of Medical Genetics|May 3, 1996
Clinical and ultrastructural findings in three patients with geleophysic dysplasiaB F Pontz, H Stöss, F Henschke, et al.
Klinische Wochenschrift|October 1, 1974
A constitutional disorder of connective tissue suggesting a defect in collagen biosynthesisW N Meigel, P K Müller, B F Pontz, et al.
Nature Genetics|April 1, 1993
Kniest and Stickler dysplasia phenotypes caused by collagen type II gene (COL2A1) defectA Winterpacht, M Hilbert, U Schwarze, et al.
Pageof 25