Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

W G Cole

Showing results (61-70 of 210) with videos related to

Pageof 21
Sort By:
The Journal of Bone and Joint Surgery. British Volume|July 1, 1992
Open fractures of the tibia in childrenP G Hope, W G Cole
Journal of Pediatric Orthopedics|July 21, 1999
Treatment of aneurysmal bone cysts with saucerization and bone marrow injection in childrenS S Hemmadi, W G Cole
Australian Veterinary Journal|January 1, 1983
Heritable bone fragility, joint laxity and dysplastic dentin in Friesian calves: a bovine syndrome of osteogenesis imperfectaL J Denholm, W G Cole
Journal of Pediatric Orthopedics|February 4, 1998
Management of subtrochanteric fractures of the femur in childrenT N Theologis, W G Cole
The Australian and New Zealand Journal of Surgery|April 1, 1988
Regulation and organization of connective tissuesW G Cole, J F Bateman
Annals of the New York Academy of Sciences|June 8, 1996
Recurrent transition at a CG dinucleotide in exon 12 of COL2A1 produces kniest dysplasia with abnormal RNA splicing by chondrocytes and lymphoblasts and interruption of the triple helix of type II collagenL Chen, W Yang, W G Cole
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|September 1, 1996
Alternative splicing of exon 12 of the COL2A1 gene interrupts the triple helix of type-II collagen in the Kniest form of spondyloepiphyseal dysplasiaL Chen, W Yang, W G Cole
Human Mutation|January 1, 1995
A novel G1006A substitution in the alpha 2(I) chain of type I collagen produces osteogenesis imperfecta type IIIJ Lu, T Costa, W G Cole
Human Mutation|February 6, 1998
Pseudoachondroplasia due to the substitution of the highly conserved Asp482 by Gly in the seventh calmodulin-like repeat of cartilage oligomeric matrix proteinS Susic, J Ahier, W G Cole
Human Mutation|January 1, 1996
A novel G499D substitution in the alpha 1(III) chain of type III collagen produces variable forms of Ehlers-Danlos syndrome type IVJ McGrory, T Costa, W G Cole
Pageof 21

Showing results (61-70 of 210) with videos related to

Sort By:
Pageof 21
The Journal of Bone and Joint Surgery. British Volume|July 1, 1992
Open fractures of the tibia in childrenP G Hope, W G Cole
Journal of Pediatric Orthopedics|July 21, 1999
Treatment of aneurysmal bone cysts with saucerization and bone marrow injection in childrenS S Hemmadi, W G Cole
Australian Veterinary Journal|January 1, 1983
Heritable bone fragility, joint laxity and dysplastic dentin in Friesian calves: a bovine syndrome of osteogenesis imperfectaL J Denholm, W G Cole
Journal of Pediatric Orthopedics|February 4, 1998
Management of subtrochanteric fractures of the femur in childrenT N Theologis, W G Cole
The Australian and New Zealand Journal of Surgery|April 1, 1988
Regulation and organization of connective tissuesW G Cole, J F Bateman
Annals of the New York Academy of Sciences|June 8, 1996
Recurrent transition at a CG dinucleotide in exon 12 of COL2A1 produces kniest dysplasia with abnormal RNA splicing by chondrocytes and lymphoblasts and interruption of the triple helix of type II collagenL Chen, W Yang, W G Cole
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society|September 1, 1996
Alternative splicing of exon 12 of the COL2A1 gene interrupts the triple helix of type-II collagen in the Kniest form of spondyloepiphyseal dysplasiaL Chen, W Yang, W G Cole
Human Mutation|January 1, 1995
A novel G1006A substitution in the alpha 2(I) chain of type I collagen produces osteogenesis imperfecta type IIIJ Lu, T Costa, W G Cole
Human Mutation|February 6, 1998
Pseudoachondroplasia due to the substitution of the highly conserved Asp482 by Gly in the seventh calmodulin-like repeat of cartilage oligomeric matrix proteinS Susic, J Ahier, W G Cole
Human Mutation|January 1, 1996
A novel G499D substitution in the alpha 1(III) chain of type III collagen produces variable forms of Ehlers-Danlos syndrome type IVJ McGrory, T Costa, W G Cole
Pageof 21