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F M Pope

Showing results (101-110 of 168) with videos related to

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Lancet (London, England)|May 2, 1981
Some patients with cerebral aneurysms are deficient in type III collagenF M Pope, A C Nicholls, P Narcisi, et al.
Clinical and Experimental Dermatology|September 1, 1991
Lipoid proteinosis--new immunopathological observationsJ A Newton, S Rasbridge, A Temple, et al.
Journal of Medical Genetics|June 1, 1992
Detection and characterisation of an overmodified type III collagen by analysis of non-cutaneous connective tissues in a patient with Ehlers-Danlos syndrome IVL Nuytinck, P Narcisi, A Nicholls, et al.
British Medical Journal (Clinical Research Ed.)|February 11, 1984
Lethal osteogenesis imperfecta congenita and a 300 base pair gene deletion for an alpha 1(I)-like collagenF M Pope, K S Cheah, A C Nicholls, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|March 1, 1994
Fibrillin secretion and microfibril assembly by Marfan dermal fibroblastsC M Kielty, J E Phillips, A H Child, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|November 1, 1996
Masked confirmation of linkage between type 1 congenital vitreous anomaly and COL 2A1 in Stickler syndromeM P Snead, J R Yates, F M Pope, et al.
Clinical and Experimental Dermatology|July 1, 1997
Genetic linkage to the collagen alpha 1 (V) gene (COL5A1) in two British Ehlers-Danlos syndrome families with variable type I and II phenotypesN P Burrows, A C Nicholls, J R Yates, et al.
Journal of Clinical Pathology|June 1, 1980
Osteogenesis imperfecta (lethal) bones contain types III and V collagensF M Pope, A C Nicholls, C Eggleton, et al.
Human Molecular Genetics|September 1, 1994
A novel homozygous point mutation in the collagen VII gene (COL7A1) in two cousins with recessive dystrophic epidermolysis bullosaM G Dunnill, A J Richards, G Milana, et al.
Current Problems in Dermatology|January 1, 1987
Clinical and genetic heterogeneity of the Marfan syndromeF M Pope, A C Nicholls, R M Lewkonia, et al.
Pageof 17

Showing results (101-110 of 168) with videos related to

Sort By:
Pageof 17
Lancet (London, England)|May 2, 1981
Some patients with cerebral aneurysms are deficient in type III collagenF M Pope, A C Nicholls, P Narcisi, et al.
Clinical and Experimental Dermatology|September 1, 1991
Lipoid proteinosis--new immunopathological observationsJ A Newton, S Rasbridge, A Temple, et al.
Journal of Medical Genetics|June 1, 1992
Detection and characterisation of an overmodified type III collagen by analysis of non-cutaneous connective tissues in a patient with Ehlers-Danlos syndrome IVL Nuytinck, P Narcisi, A Nicholls, et al.
British Medical Journal (Clinical Research Ed.)|February 11, 1984
Lethal osteogenesis imperfecta congenita and a 300 base pair gene deletion for an alpha 1(I)-like collagenF M Pope, K S Cheah, A C Nicholls, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|March 1, 1994
Fibrillin secretion and microfibril assembly by Marfan dermal fibroblastsC M Kielty, J E Phillips, A H Child, et al.
Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|November 1, 1996
Masked confirmation of linkage between type 1 congenital vitreous anomaly and COL 2A1 in Stickler syndromeM P Snead, J R Yates, F M Pope, et al.
Clinical and Experimental Dermatology|July 1, 1997
Genetic linkage to the collagen alpha 1 (V) gene (COL5A1) in two British Ehlers-Danlos syndrome families with variable type I and II phenotypesN P Burrows, A C Nicholls, J R Yates, et al.
Journal of Clinical Pathology|June 1, 1980
Osteogenesis imperfecta (lethal) bones contain types III and V collagensF M Pope, A C Nicholls, C Eggleton, et al.
Human Molecular Genetics|September 1, 1994
A novel homozygous point mutation in the collagen VII gene (COL7A1) in two cousins with recessive dystrophic epidermolysis bullosaM G Dunnill, A J Richards, G Milana, et al.
Current Problems in Dermatology|January 1, 1987
Clinical and genetic heterogeneity of the Marfan syndromeF M Pope, A C Nicholls, R M Lewkonia, et al.
Pageof 17