J E Craig - JoVE Visualize

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Search research articles

ABOUT JoVE

Overview Leadership Blog JoVE Help Center

AUTHORS

Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

LIBRARIANS

Testimonials Subscriptions Access Resources Library Advisory Board FAQ

RESEARCH

JoVE Journal Methods Collections JoVE Encyclopedia of Experiments Archive

EDUCATION

JoVE Core JoVE Business JoVE Science Education JoVE Lab Manual Faculty Resource Center Faculty Site

Terms & Conditions of Use

Policies

Filters

J E Craig

Showing results (51-60 of 53) with videos related to

Pageof 6

Sort By:

You have reached the last page of results.This site can display upto 53 results.

Ophthalmology|September 6, 2001

Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifierJ E Craig, P N Baird, D L Healey, et al.

Human Molecular Genetics|July 7, 2001

Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophyC Toomes, N J Marchbank, D A Mackey, et al.

Human Molecular Genetics|April 10, 1999

Analysis of myocilin mutations in 1703 glaucoma patients from five different populationsJ H Fingert, E Héon, J M Liebmann, et al.

Pageof 6

Search research articles

Showing results (51-60 of 53) with videos related to

Sort By:

Pageof 6

You have reached the last page of results.This site can display upto 53 results.

Ophthalmology|September 6, 2001

Evidence for genetic heterogeneity within eight glaucoma families, with the GLC1A Gln368STOP mutation being an important phenotypic modifierJ E Craig, P N Baird, D L Healey, et al.

Human Molecular Genetics|July 7, 2001

Spectrum, frequency and penetrance of OPA1 mutations in dominant optic atrophyC Toomes, N J Marchbank, D A Mackey, et al.

Human Molecular Genetics|April 10, 1999

Analysis of myocilin mutations in 1703 glaucoma patients from five different populationsJ H Fingert, E Héon, J M Liebmann, et al.

Pageof 6