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

S J Knight

Showing results (11-20 of 51) with videos related to

Pageof 6
Sort By:
Clinical Science (London, England : 1979)|September 1, 1992
The fragile X syndromeM C Hirst, S J Knight, M V Bell, et al.
American Journal of Medical Genetics|February 7, 1998
Population genetics of the FRAXE and FRAXF GCC repeats, and a novel CGG repeat, in Xq28R J Ritchie, L Chakrabarti, S J Knight, et al.
Biochimica Et Biophysica Acta|June 9, 1995
The fragile X syndromeA V Flannery, M C Hirst, S J Knight, et al.
Osteoarthritis and Cartilage|December 8, 2016
Patient-specific chondrolabral contact mechanics in patients with acetabular dysplasia following treatment with peri-acetabular osteotomyC L Abraham, S J Knight, C L Peters, et al.
BMC Surgery|May 21, 2022
Patients undergoing colorectal surgery at a Veterans Affairs Hospital do not experience racial disparity in length of stay either before or after implementing an enhanced recovery pathwayC Rentas, S Baker, L Goss, et al.
Journal of Clinical Psychology in Medical Settings|November 15, 2013
Coping strategies and psychological distress in cancer patients before autologous bone marrow transplantJ J Mytko, S J Knight, D Chastain, et al.
Prenatal Diagnosis|July 23, 1999
A case of recurrent congenital fetal anomalies associated with a familial subtelomeric translocationK J Brackley, M D Kilby, J Morton, et al.
Journal of Medical Genetics|May 19, 2001
Submicroscopic subtelomeric 1qter deletions: a recognisable phenotype?B B De Vries, S J Knight, T Homfray, et al.
American Journal of Human Genetics|July 1, 1994
Triplet repeat expansion at the FRAXE locus and X-linked mild mental handicapS J Knight, M A Voelckel, M C Hirst, et al.
Journal of Medical Genetics|August 1, 1993
Origins of the fragile X syndrome mutationM C Hirst, S J Knight, Z Christodoulou, et al.
Pageof 6

Showing results (11-20 of 51) with videos related to

Sort By:
Pageof 6
Clinical Science (London, England : 1979)|September 1, 1992
The fragile X syndromeM C Hirst, S J Knight, M V Bell, et al.
American Journal of Medical Genetics|February 7, 1998
Population genetics of the FRAXE and FRAXF GCC repeats, and a novel CGG repeat, in Xq28R J Ritchie, L Chakrabarti, S J Knight, et al.
Biochimica Et Biophysica Acta|June 9, 1995
The fragile X syndromeA V Flannery, M C Hirst, S J Knight, et al.
Osteoarthritis and Cartilage|December 8, 2016
Patient-specific chondrolabral contact mechanics in patients with acetabular dysplasia following treatment with peri-acetabular osteotomyC L Abraham, S J Knight, C L Peters, et al.
BMC Surgery|May 21, 2022
Patients undergoing colorectal surgery at a Veterans Affairs Hospital do not experience racial disparity in length of stay either before or after implementing an enhanced recovery pathwayC Rentas, S Baker, L Goss, et al.
Journal of Clinical Psychology in Medical Settings|November 15, 2013
Coping strategies and psychological distress in cancer patients before autologous bone marrow transplantJ J Mytko, S J Knight, D Chastain, et al.
Prenatal Diagnosis|July 23, 1999
A case of recurrent congenital fetal anomalies associated with a familial subtelomeric translocationK J Brackley, M D Kilby, J Morton, et al.
Journal of Medical Genetics|May 19, 2001
Submicroscopic subtelomeric 1qter deletions: a recognisable phenotype?B B De Vries, S J Knight, T Homfray, et al.
American Journal of Human Genetics|July 1, 1994
Triplet repeat expansion at the FRAXE locus and X-linked mild mental handicapS J Knight, M A Voelckel, M C Hirst, et al.
Journal of Medical Genetics|August 1, 1993
Origins of the fragile X syndrome mutationM C Hirst, S J Knight, Z Christodoulou, et al.
Pageof 6