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

I McIntosh

Showing results (51-60 of 97) with videos related to

Pageof 10
Sort By:
Human Genetics|September 1, 1990
The haplotype distribution of the delta F508 mutation in cystic fibrosis families in ScotlandI McIntosh, A Curtis, M L Lorenzo, et al.
Computer Assisted Surgery (Abingdon, England)|October 18, 2023
Improving alignment in total knee arthroplasty: a cadaveric assessment of a surgical navigation tool with computed tomography imagingKelly A Foley, Ran Schwarzkopf, Brian M Culp, et al.
The Journal of Clinical Investigation|October 15, 1996
Glanzmann thrombasthenia. Cooperation between sequence variants in cis during splice site selectionY Jin, H C Dietz, R A Montgomery, et al.
Clinical Science (London, England : 1979)|January 1, 1992
Increased energy expenditure in cystic fibrosis is associated with specific mutationsA O'Rawe, I McIntosh, J A Dodge, et al.
Genetic Epidemiology|January 5, 2002
Testing candidate genes for non-syndromic oral clefts using a case-parent trio designTerri H Beaty, J B Hetmanski, J S Zeiger, et al.
Human Genetics|August 11, 1992
Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) geneL Osborne, G Santis, M Schwarz, et al.
Genomics|August 1, 1993
Four novel FBN1 mutations: significance for mutant transcript level and EGF-like domain calcium binding in the pathogenesis of Marfan syndromeH C Dietz, I McIntosh, L Y Sakai, et al.
Human Molecular Genetics|June 9, 1998
Loss-of-function mutations in the LIM-homeodomain gene, LMX1B, in nail-patella syndromeD Vollrath, V L Jaramillo-Babb, M V Clough, et al.
Arthroplasty Today|January 31, 2024
The Hip-spine Assessment of a Novel Surgical Planning Software Provides Acetabular Component Targets That Are Reliable and in Agreement With Current Clinical RecommendationsEmily I McIntosh, Nana O Sarpong, John R Steele, et al.
Human Molecular Genetics|June 1, 1994
Substitution of a cysteine residue in a non-calcium binding, EGF-like domain of fibrillin segregates with the Marfan syndrome in a large kindredL D Piersall, H C Dietz, B D Hall, et al.
Pageof 10

Showing results (51-60 of 97) with videos related to

Sort By:
Pageof 10
Human Genetics|September 1, 1990
The haplotype distribution of the delta F508 mutation in cystic fibrosis families in ScotlandI McIntosh, A Curtis, M L Lorenzo, et al.
Computer Assisted Surgery (Abingdon, England)|October 18, 2023
Improving alignment in total knee arthroplasty: a cadaveric assessment of a surgical navigation tool with computed tomography imagingKelly A Foley, Ran Schwarzkopf, Brian M Culp, et al.
The Journal of Clinical Investigation|October 15, 1996
Glanzmann thrombasthenia. Cooperation between sequence variants in cis during splice site selectionY Jin, H C Dietz, R A Montgomery, et al.
Clinical Science (London, England : 1979)|January 1, 1992
Increased energy expenditure in cystic fibrosis is associated with specific mutationsA O'Rawe, I McIntosh, J A Dodge, et al.
Genetic Epidemiology|January 5, 2002
Testing candidate genes for non-syndromic oral clefts using a case-parent trio designTerri H Beaty, J B Hetmanski, J S Zeiger, et al.
Human Genetics|August 11, 1992
Incidence and expression of the N1303K mutation of the cystic fibrosis (CFTR) geneL Osborne, G Santis, M Schwarz, et al.
Genomics|August 1, 1993
Four novel FBN1 mutations: significance for mutant transcript level and EGF-like domain calcium binding in the pathogenesis of Marfan syndromeH C Dietz, I McIntosh, L Y Sakai, et al.
Human Molecular Genetics|June 9, 1998
Loss-of-function mutations in the LIM-homeodomain gene, LMX1B, in nail-patella syndromeD Vollrath, V L Jaramillo-Babb, M V Clough, et al.
Arthroplasty Today|January 31, 2024
The Hip-spine Assessment of a Novel Surgical Planning Software Provides Acetabular Component Targets That Are Reliable and in Agreement With Current Clinical RecommendationsEmily I McIntosh, Nana O Sarpong, John R Steele, et al.
Human Molecular Genetics|June 1, 1994
Substitution of a cysteine residue in a non-calcium binding, EGF-like domain of fibrillin segregates with the Marfan syndrome in a large kindredL D Piersall, H C Dietz, B D Hall, et al.
Pageof 10