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F M Pope

Showing results (161-170 of 168) with videos related to

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Clinical and Experimental Dermatology|September 1, 1988
Type III collagen mutations in Ehlers Danlos syndrome type IV and other related disordersF M Pope, A C Nicholls, P Narcisi, et al.
Journal of Medical Genetics|August 1, 1984
The clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfectaA C Nicholls, G Osse, H G Schloon, et al.
Journal of Medical Genetics|September 3, 2002
Vitreoretinopathy with phalangeal epiphyseal dysplasia, a type II collagenopathy resulting from a novel mutation in the C-propeptide region of the moleculeA J Richards, J Morgan, P W P Bearcroft, et al.
British Journal of Neurosurgery|January 1, 1991
Type III collagen mutations cause fragile cerebral arteriesF M Pope, B E Kendall, G I Slapak, et al.
Nature Genetics|June 3, 2000
Mutations in a gene encoding an ABC transporter cause pseudoxanthoma elasticumO Le Saux, Z Urban, C Tschuch, et al.
American Journal of Human Genetics|September 6, 2001
A spectrum of ABCC6 mutations is responsible for pseudoxanthoma elasticumO Le Saux, K Beck, C Sachsinger, et al.
Genomics|December 10, 1999
Pseudoxanthoma elasticum maps to an 820-kb region of the p13.1 region of chromosome 16O Le Saux, Z Urban, H H Göring, et al.
Frontiers in Genetics|June 16, 2023
Non-oral manifestations in adults with a clinical and molecularly confirmed diagnosis of periodontal Ehlers-Danlos syndromeC Angwin, J Zschocke, T Kammin, et al.
Pageof 17

Showing results (161-170 of 168) with videos related to

Sort By:
Pageof 17
You have reached the last page of results.This site can display upto 168 results.
Clinical and Experimental Dermatology|September 1, 1988
Type III collagen mutations in Ehlers Danlos syndrome type IV and other related disordersF M Pope, A C Nicholls, P Narcisi, et al.
Journal of Medical Genetics|August 1, 1984
The clinical features of homozygous alpha 2(I) collagen deficient osteogenesis imperfectaA C Nicholls, G Osse, H G Schloon, et al.
Journal of Medical Genetics|September 3, 2002
Vitreoretinopathy with phalangeal epiphyseal dysplasia, a type II collagenopathy resulting from a novel mutation in the C-propeptide region of the moleculeA J Richards, J Morgan, P W P Bearcroft, et al.
British Journal of Neurosurgery|January 1, 1991
Type III collagen mutations cause fragile cerebral arteriesF M Pope, B E Kendall, G I Slapak, et al.
Nature Genetics|June 3, 2000
Mutations in a gene encoding an ABC transporter cause pseudoxanthoma elasticumO Le Saux, Z Urban, C Tschuch, et al.
American Journal of Human Genetics|September 6, 2001
A spectrum of ABCC6 mutations is responsible for pseudoxanthoma elasticumO Le Saux, K Beck, C Sachsinger, et al.
Genomics|December 10, 1999
Pseudoxanthoma elasticum maps to an 820-kb region of the p13.1 region of chromosome 16O Le Saux, Z Urban, H H Göring, et al.
Frontiers in Genetics|June 16, 2023
Non-oral manifestations in adults with a clinical and molecularly confirmed diagnosis of periodontal Ehlers-Danlos syndromeC Angwin, J Zschocke, T Kammin, et al.
Pageof 17