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M A Musarella

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Nature Genetics|November 4, 2000

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindnessN T Bech-Hansen, M J Naylor, T A Maybaum, et al.

Ophthalmology|October 1, 1998

Novel trabecular meshwork inducible glucocorticoid response mutation in an eight-generation juvenile-onset primary open-angle glaucoma pedigreeJ E Richards, R Ritch, P R Lichter, et al.

American Journal of Human Genetics|June 13, 1998

OA1 mutations and deletions in X-linked ocular albinismR E Schnur, M Gao, P A Wick, et al.

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Search research articles

Showing results (41-50 of 43) with videos related to

Sort By:

Pageof 5

You have reached the last page of results.This site can display upto 43 results.

Nature Genetics|November 4, 2000

Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindnessN T Bech-Hansen, M J Naylor, T A Maybaum, et al.

Ophthalmology|October 1, 1998

Novel trabecular meshwork inducible glucocorticoid response mutation in an eight-generation juvenile-onset primary open-angle glaucoma pedigreeJ E Richards, R Ritch, P R Lichter, et al.

American Journal of Human Genetics|June 13, 1998

OA1 mutations and deletions in X-linked ocular albinismR E Schnur, M Gao, P A Wick, et al.

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