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

Tim K Footz

Showing results (1-10 of 4) with videos related to

Pageof 1
Sort By:
Human Genetics|December 17, 2002
Three duplicons form a novel chimeric transcription unit in the pericentromeric region of chromosome 22q11Lindsay Bridgland, Tim K Footz, Melanie D Kardel, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 11, 2007
Analyses of a novel L130F missense mutation in FOXC1Yoko A Ito, Tim K Footz, Tara C Murphy, et al.
Human Molecular Genetics|January 20, 2009
Glaucoma-associated WDR36 variants encode functional defects in a yeast model systemTim K Footz, Jill L Johnson, Stéphane Dubois, et al.
Investigative Ophthalmology & Visual Science|March 13, 2009
Severe molecular defects of a novel FOXC1 W152G mutation result in aniridiaYoko A Ito, Tim K Footz, Fred B Berry, et al.
Pageof 1

Showing results (1-10 of 4) with videos related to

Sort By:
Pageof 1
Human Genetics|December 17, 2002
Three duplicons form a novel chimeric transcription unit in the pericentromeric region of chromosome 22q11Lindsay Bridgland, Tim K Footz, Melanie D Kardel, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|January 11, 2007
Analyses of a novel L130F missense mutation in FOXC1Yoko A Ito, Tim K Footz, Tara C Murphy, et al.
Human Molecular Genetics|January 20, 2009
Glaucoma-associated WDR36 variants encode functional defects in a yeast model systemTim K Footz, Jill L Johnson, Stéphane Dubois, et al.
Investigative Ophthalmology & Visual Science|March 13, 2009
Severe molecular defects of a novel FOXC1 W152G mutation result in aniridiaYoko A Ito, Tim K Footz, Fred B Berry, et al.
Pageof 1