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R R McInnes

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Nature Genetics|April 16, 1998

De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosisC L Freund, Q L Wang, S Chen, et al.

Nature Genetics|April 1, 1996

Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiationM Burmeister, J Novak, M Y Liang, et al.

Nature Genetics|August 10, 2000

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10E Ferda Percin, L A Ploder, J J Yu, et al.

Cell|December 9, 1997

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptorC L Freund, C Y Gregory-Evans, T Furukawa, et al.

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Search research articles

Showing results (71-80 of 74) with videos related to

Sort By:

Pageof 8

You have reached the last page of results.This site can display upto 74 results.

Nature Genetics|April 16, 1998

De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosisC L Freund, Q L Wang, S Chen, et al.

Nature Genetics|April 1, 1996

Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiationM Burmeister, J Novak, M Y Liang, et al.

Nature Genetics|August 10, 2000

Human microphthalmia associated with mutations in the retinal homeobox gene CHX10E Ferda Percin, L A Ploder, J J Yu, et al.

Cell|December 9, 1997

Cone-rod dystrophy due to mutations in a novel photoreceptor-specific homeobox gene (CRX) essential for maintenance of the photoreceptorC L Freund, C Y Gregory-Evans, T Furukawa, et al.

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