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F M Pope

Showing results (91-100 of 168) with videos related to

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Lancet (London, England)|April 23, 1983
Aortic compliance in patients with ruptured intracranial aneurysmsG Neil-Dwyer, A H Child, D E Dorrance, et al.
Human Genetics|March 1, 1992
The molecular defect in a family with mild atypical osteogenesis imperfecta and extreme joint hypermobility: exon skipping caused by an 11-bp deletion from an intron in one COL1A2 alleleA C Nicholls, J Oliver, D V Renouf, et al.
Clinical and Experimental Dermatology|May 16, 2013
Palmoplantar contractures in childhood: a rare complication of vascular Ehlers-Danlos syndromeA C Foulkes, R Pollitt, G Sobey, et al.
Collagen and Related Research|October 1, 1984
Presence of translatable mRNA for pro alpha 2(I) chains in fibroblasts from a patient with osteogenesis imperfecta whose type I collagen does not contain alpha 2(I) chainsM L Chu, D Rowe, A C Nicholls, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Prenatal diagnosis and prevention of inherited abnormalities of collagenF M Pope, S C Daw, P Narcisi, et al.
Nucleic Acids Research|July 11, 1985
A highly polymorphic region 3' to the human type II collagen geneN G Stoker, K S Cheah, J R Griffin, et al.
The British Journal of Dermatology|August 1, 1996
COL3A1 mutations cause variable clinical phenotypes including acrogeria and vascular ruptureF M Pope, P Narcisi, A C Nicholls, et al.
Human Genetics|June 1, 1991
Ehlers-Danlos syndrome type VII: a single base change that causes exon skipping in the type I collagen alpha 2(I) chainA C Nicholls, J Oliver, D V Renouf, et al.
Molecular Biology & Medicine|December 1, 1988
A cysteine for glycine substitution at position 1017 in an alpha 1(I) chain of type I collagen in a patient with mild dominantly inherited osteogenesis imperfectaM E Labhard, M K Wirtz, F M Pope, et al.
Human Mutation|January 1, 1995
Efficient strategy for the detection of mutations in acrogeric Ehlers-Danlos syndrome type IVP H Johnson, A J Richards, J C Lloyd, et al.
Pageof 17

Showing results (91-100 of 168) with videos related to

Sort By:
Pageof 17
Lancet (London, England)|April 23, 1983
Aortic compliance in patients with ruptured intracranial aneurysmsG Neil-Dwyer, A H Child, D E Dorrance, et al.
Human Genetics|March 1, 1992
The molecular defect in a family with mild atypical osteogenesis imperfecta and extreme joint hypermobility: exon skipping caused by an 11-bp deletion from an intron in one COL1A2 alleleA C Nicholls, J Oliver, D V Renouf, et al.
Clinical and Experimental Dermatology|May 16, 2013
Palmoplantar contractures in childhood: a rare complication of vascular Ehlers-Danlos syndromeA C Foulkes, R Pollitt, G Sobey, et al.
Collagen and Related Research|October 1, 1984
Presence of translatable mRNA for pro alpha 2(I) chains in fibroblasts from a patient with osteogenesis imperfecta whose type I collagen does not contain alpha 2(I) chainsM L Chu, D Rowe, A C Nicholls, et al.
Journal of Inherited Metabolic Disease|January 1, 1989
Prenatal diagnosis and prevention of inherited abnormalities of collagenF M Pope, S C Daw, P Narcisi, et al.
Nucleic Acids Research|July 11, 1985
A highly polymorphic region 3' to the human type II collagen geneN G Stoker, K S Cheah, J R Griffin, et al.
The British Journal of Dermatology|August 1, 1996
COL3A1 mutations cause variable clinical phenotypes including acrogeria and vascular ruptureF M Pope, P Narcisi, A C Nicholls, et al.
Human Genetics|June 1, 1991
Ehlers-Danlos syndrome type VII: a single base change that causes exon skipping in the type I collagen alpha 2(I) chainA C Nicholls, J Oliver, D V Renouf, et al.
Molecular Biology & Medicine|December 1, 1988
A cysteine for glycine substitution at position 1017 in an alpha 1(I) chain of type I collagen in a patient with mild dominantly inherited osteogenesis imperfectaM E Labhard, M K Wirtz, F M Pope, et al.
Human Mutation|January 1, 1995
Efficient strategy for the detection of mutations in acrogeric Ehlers-Danlos syndrome type IVP H Johnson, A J Richards, J C Lloyd, et al.
Pageof 17