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G Tromp

Showing results (1-10 of 80) with videos related to

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Journal of Vascular Surgery|May 1, 1992
DNA sequencing as a method to identify mutations in patients with familial forms of aneurysmsG Tromp, H Kuivaniemi
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1991
[Are arterial aneurysms hereditary?]H Kuivaniemi, G Tromp
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|September 29, 2009
Developments in genomics to improve understanding, diagnosis and management of aneurysms and peripheral artery diseaseG Tromp, H Kuivaniemi
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1988
Single base mutation in the pro alpha 2(I) collagen gene that causes efficient splicing of RNA from exon 27 to exon 29 and synthesis of a shortened but in-frame pro alpha 2(I) chainG Tromp, D J Prockop
Neurosurgery|July 1, 1995
Special features of familial intracranial aneurysms: report of 215 familial aneurysmsA Ronkainen, J Hernesniemi, G Tromp
Human Mutation|January 1, 1997
Mutations in fibrillar collagens (types I, II, III, and XI), fibril-associated collagen (type IX), and network-forming collagen (type X) cause a spectrum of diseases of bone, cartilage, and blood vesselsH Kuivaniemi, G Tromp, D J Prockop
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 1, 1991
Mutations in collagen genes: causes of rare and some common diseases in humansH Kuivaniemi, G Tromp, D J Prockop
Clinics in Plastic Surgery|July 1, 1994
Molecular basis of osteogenesis imperfecta and related disorders of boneD J Prockop, H Kuivaniemi, G Tromp
The Journal of Clinical Investigation|November 1, 1991
Genetic causes of aortic aneurysms. Unlearning at least part of what the textbooks sayH Kuivaniemi, G Tromp, D J Prockop
The Journal of Biological Chemistry|November 15, 1989
The brown alga Ascophyllum nodosum contains two different vanadium bromoperoxidasesB E Krenn, M G Tromp, R Wever
Pageof 8

Showing results (1-10 of 80) with videos related to

Sort By:
Pageof 8
Journal of Vascular Surgery|May 1, 1992
DNA sequencing as a method to identify mutations in patients with familial forms of aneurysmsG Tromp, H Kuivaniemi
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1991
[Are arterial aneurysms hereditary?]H Kuivaniemi, G Tromp
European Journal of Vascular and Endovascular Surgery : the Official Journal of the European Society for Vascular Surgery|September 29, 2009
Developments in genomics to improve understanding, diagnosis and management of aneurysms and peripheral artery diseaseG Tromp, H Kuivaniemi
Proceedings of the National Academy of Sciences of the United States of America|July 1, 1988
Single base mutation in the pro alpha 2(I) collagen gene that causes efficient splicing of RNA from exon 27 to exon 29 and synthesis of a shortened but in-frame pro alpha 2(I) chainG Tromp, D J Prockop
Neurosurgery|July 1, 1995
Special features of familial intracranial aneurysms: report of 215 familial aneurysmsA Ronkainen, J Hernesniemi, G Tromp
Human Mutation|January 1, 1997
Mutations in fibrillar collagens (types I, II, III, and XI), fibril-associated collagen (type IX), and network-forming collagen (type X) cause a spectrum of diseases of bone, cartilage, and blood vesselsH Kuivaniemi, G Tromp, D J Prockop
FASEB Journal : Official Publication of the Federation of American Societies for Experimental Biology|April 1, 1991
Mutations in collagen genes: causes of rare and some common diseases in humansH Kuivaniemi, G Tromp, D J Prockop
Clinics in Plastic Surgery|July 1, 1994
Molecular basis of osteogenesis imperfecta and related disorders of boneD J Prockop, H Kuivaniemi, G Tromp
The Journal of Clinical Investigation|November 1, 1991
Genetic causes of aortic aneurysms. Unlearning at least part of what the textbooks sayH Kuivaniemi, G Tromp, D J Prockop
The Journal of Biological Chemistry|November 15, 1989
The brown alga Ascophyllum nodosum contains two different vanadium bromoperoxidasesB E Krenn, M G Tromp, R Wever
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