F M Pope|A C Nicholls - JoVE Visualize

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The British Journal of Dermatology|September 1, 1984

Ehlers-Danlos syndrome type IV mimicking non-accidental injury in a childD L Roberts, F M Pope, A C Nicholls, et al.

Human Mutation|January 1, 1996

Mutation in the carboxy-terminal propeptide of the Pro alpha 1(I) chain of type I collagen in a child with severe osteogenesis imperfecta (OI type III): possible implications for protein foldingJ E Oliver, E M Thompson, F M Pope, et al.

Journal of Medical Genetics|December 1, 1985

Collagen genes and proteins in osteogenesis imperfectaF M Pope, A C Nicholls, J McPheat, et al.

Journal of Medical Genetics|November 1, 1991

Substitution of cysteine for glycine at residue 415 of one allele of the alpha 1(I) chain of type I procollagen in type III/IV osteogenesis imperfectaA C Nicholls, J Oliver, D V Renouf, et al.

Archives of Disease in Childhood|September 1, 1988

Clinical presentations of Ehlers Danlos syndrome type IVF M Pope, P Narcisi, A C Nicholls, et al.

Human Mutation|January 1, 1996

Splice site mutation causing deletion of exon 21 sequences from the pro alpha 2(I) chain of type I collagen in a patient with severe dentinogenesis imperfecta but very mild osteogenesis imperfectaA C Nicholls, J Oliver, S McCarron, et al.

Journal of Neurosurgery|July 1, 1983

Collagen deficiency and ruptured cerebral aneurysms. A clinical and biochemical studyG Neil-Dwyer, J R Bartlett, A C Nicholls, et al.

Journal of the Royal Society of Medicine|March 1, 1980

EDS IV (acrogeria): new autosomal dominant and recessive typesF M Pope, A C Nicholls, P M Jones, 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.

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.

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Showing results (1-10 of 119) with videos related to

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Pageof 12

The British Journal of Dermatology|September 1, 1984

Ehlers-Danlos syndrome type IV mimicking non-accidental injury in a childD L Roberts, F M Pope, A C Nicholls, et al.

Human Mutation|January 1, 1996

Mutation in the carboxy-terminal propeptide of the Pro alpha 1(I) chain of type I collagen in a child with severe osteogenesis imperfecta (OI type III): possible implications for protein foldingJ E Oliver, E M Thompson, F M Pope, et al.

Journal of Medical Genetics|December 1, 1985

Collagen genes and proteins in osteogenesis imperfectaF M Pope, A C Nicholls, J McPheat, et al.

Journal of Medical Genetics|November 1, 1991

Substitution of cysteine for glycine at residue 415 of one allele of the alpha 1(I) chain of type I procollagen in type III/IV osteogenesis imperfectaA C Nicholls, J Oliver, D V Renouf, et al.

Archives of Disease in Childhood|September 1, 1988

Clinical presentations of Ehlers Danlos syndrome type IVF M Pope, P Narcisi, A C Nicholls, et al.

Human Mutation|January 1, 1996

Splice site mutation causing deletion of exon 21 sequences from the pro alpha 2(I) chain of type I collagen in a patient with severe dentinogenesis imperfecta but very mild osteogenesis imperfectaA C Nicholls, J Oliver, S McCarron, et al.

Journal of Neurosurgery|July 1, 1983

Collagen deficiency and ruptured cerebral aneurysms. A clinical and biochemical studyG Neil-Dwyer, J R Bartlett, A C Nicholls, et al.

Journal of the Royal Society of Medicine|March 1, 1980

EDS IV (acrogeria): new autosomal dominant and recessive typesF M Pope, A C Nicholls, P M Jones, 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.

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.

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