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Publishing Process Editorial Board Scope & Policies Peer Review FAQ Submit

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G A Fishman

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Archives of Ophthalmology (Chicago, Ill. : 1960)|March 20, 2001

Mutations in the CRB1 gene cause Leber congenital amaurosisA J Lotery, S G Jacobson, G A Fishman, et al.

Investigative Ophthalmology & Visual Science|May 1, 2001

An analysis of allelic variation in the ABCA4 geneA R Webster, E Héon, A J Lotery, et al.

Archives of Ophthalmology (Chicago, Ill. : 1960)|April 15, 2000

Mutation analysis of 3 genes in patients with Leber congenital amaurosisA J Lotery, P Namperumalsamy, S G Jacobson, et al.

Nature Genetics|February 2, 2000

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fateN B Haider, S G Jacobson, A V Cideciyan, et al.

Pageof 23

Search research articles

Showing results (221-230 of 224) with videos related to

Sort By:

Pageof 23

You have reached the last page of results.This site can display upto 224 results.

Archives of Ophthalmology (Chicago, Ill. : 1960)|March 20, 2001

Mutations in the CRB1 gene cause Leber congenital amaurosisA J Lotery, S G Jacobson, G A Fishman, et al.

Investigative Ophthalmology & Visual Science|May 1, 2001

An analysis of allelic variation in the ABCA4 geneA R Webster, E Héon, A J Lotery, et al.

Archives of Ophthalmology (Chicago, Ill. : 1960)|April 15, 2000

Mutation analysis of 3 genes in patients with Leber congenital amaurosisA J Lotery, P Namperumalsamy, S G Jacobson, et al.

Nature Genetics|February 2, 2000

Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fateN B Haider, S G Jacobson, A V Cideciyan, et al.

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